Zimmer Biomet Receives FDA Approval for Oxford® Cementless Partial Knee, Only Cementless Partial Knee Replacement Implant in the U.S.
Zimmer Biomet has received FDA approval for the Oxford® Cementless Partial Knee, making it the only cementless partial knee replacement implant available in the U.S. The approval is based on safety and effectiveness data from an IDE study. The device offers improved fixation, better long-term implant survival, and enhanced operating room efficiency compared to cemented procedures. With over 20 years of clinical experience and 300,000+ procedures worldwide, the implant features a mobile bearing design that mimics natural knee movement. The UK registry shows a 94.1% implant survival rate at 10 years, surpassing the average for other partial knees. U.S. launch is planned for Q1 2025.
Zimmer Biomet ha ricevuto l'approvazione della FDA per il Oxford® Cementless Partial Knee, rendendolo l'unico impianto di sostituzione parziale del ginocchio senza cemento disponibile negli Stati Uniti. L'approvazione si basa su dati di sicurezza ed efficacia provenienti da uno studio IDE. Il dispositivo offre un miglioramento della fissazione, una maggiore sopravvivenza a lungo termine dell'impianto e una maggiore efficienza in sala operatoria rispetto alle procedure cementate. Con oltre 20 anni di esperienza clinica e oltre 300.000 procedure in tutto il mondo, l'impianto presenta un design a supporto mobile che imita il movimento naturale del ginocchio. Il registro del Regno Unito mostra una percentuale di sopravvivenza dell'impianto del 94,1% dopo 10 anni, superando la media di altri ginocchi parziali. Il lancio negli Stati Uniti è previsto per il primo trimestre del 2025.
Zimmer Biomet ha recibido la aprobación de la FDA para el Oxford® Cementless Partial Knee, convirtiéndose en el único implante de reemplazo de rodilla parcial sin cemento disponible en los EE.UU. La aprobación se basa en datos de seguridad y eficacia de un estudio IDE. El dispositivo ofrece una mejor fijación, una mayor supervivencia del implante a largo plazo y una eficiencia mejorada en la sala de operaciones en comparación con los procedimientos con cemento. Con más de 20 años de experiencia clínica y más de 300,000 procedimientos en todo el mundo, el implante presenta un diseño de soporte móvil que imita el movimiento natural de la rodilla. El registro del Reino Unido muestra una tasa de supervivencia del implante del 94,1% a los 10 años, superando el promedio de otras rodillas parciales. El lanzamiento en EE.UU. está previsto para el primer trimestre de 2025.
Zimmer Biomet는 영국식 무시멘트 부분 슬관절에 대해 FDA 승인을 받으며, 미국에서 사용 가능한 유일한 무시멘트 부분 슬관절 대체 임플란트가 되었습니다. 이 승인은 IDE 연구의 안전성 및 효과성 데이터를 기반으로 합니다. 이 장치는 시멘트 시술에 비해 개선된 고정력, 장기 임플란트 생존율, 그리고 수술실 효율성을 제공합니다. 전 세계적으로 20년 이상의 임상 경험과 300,000건 이상의 시술을 보유하고 있으며, 이 임플란트는 자연 슬관절 움직임을 모방하는 이동식 베어링 디자인을 특징으로 합니다. 영국 등록부에 따르면 10년 후 임플란트 생존율은 94.1%로, 다른 부분 슬관절의 평균을 초과합니다. 미국 출시 예정은 2025년 1분기입니다.
Zimmer Biomet a reçu l'approbation de la FDA pour le Oxford® Cementless Partial Knee, faisant de lui le seul implant de remplacement partiel du genou sans ciment disponible aux États-Unis. L'approbation repose sur des données de sécurité et d'efficacité provenant d'une étude IDE. Le dispositif offre une meilleure fixation, une survie à long terme améliorée de l'implant et une efficacité accrue en salle d'opération par rapport aux procédures cimentées. Avec plus de 20 ans d'expérience clinique et plus de 300 000 procédures dans le monde, l'implant présente un design à roulement mobile qui imite le mouvement naturel du genou. Le registre du Royaume-Uni montre un taux de survie de l'implant de 94,1 % après 10 ans, surpassant la moyenne d'autres genoux partiels. Le lancement aux États-Unis est prévu pour le premier trimestre 2025.
Zimmer Biomet hat die FDA-Zulassung für das Oxford® Cementless Partial Knee erhalten, was es zum einzigen zementfreien Teilknie-Ersatzimplantat in den USA macht. Die Zulassung basiert auf Sicherheits- und Wirksamkeitsdaten aus einer IDE-Studie. Das Gerät bietet eine verbesserte Verankerung, eine bessere Langzeit-Überlebensrate des Implantats und eine erhöhte Effizienz im Operationssaal im Vergleich zu zementierten Verfahren. Mit über 20 Jahren klinischer Erfahrung und über 300.000 Verfahren weltweit bietet das Implantat ein mobiles Lagerdesign, das die natürliche Bewegung des Knies nachahmt. Das Register des Vereinigten Königreichs zeigt eine Implantat-Überlebensrate von 94,1% nach 10 Jahren, die über dem Durchschnitt anderer Teilknie liegt. Der Start in den USA ist für das 1. Quartal 2025 geplant.
- First and only FDA-approved cementless partial knee implant in the U.S.
- 94.1% implant survival rate at 10 years, higher than industry average of 89.9%
- Proven track record with 300,000+ procedures across multiple regions
- Improved operating room efficiency and reduced costs compared to cemented procedures
- Lifetime warranty covering replacement implant costs
- to unilateral knee procedures only
- Not indicated for lateral compartment or ligament deficiency cases
- Cannot be used in simultaneous bilateral surgery
Insights
The FDA approval of Oxford® Cementless Partial Knee represents a significant market opportunity for Zimmer Biomet. This device addresses a clear gap in the U.S. market as the only FDA-approved cementless partial knee implant, backed by impressive clinical data showing
The cementless approach offers compelling advantages: improved surgical efficiency, reduced OR time and better long-term fixation. These benefits could drive adoption among surgeons and healthcare facilities looking to optimize costs and improve patient outcomes. The Q1 2025 launch timeline gives ZBH time to properly train surgeons and build a strong commercial foundation.
This approval has significant revenue implications. The partial knee replacement market segment is growing faster than total knee replacements, driven by younger, more active patients seeking less invasive options. The cementless technology's reduced OR time and elimination of cement-related costs provide compelling economic benefits for healthcare facilities. The lifetime warranty offering is a strategic differentiator that could accelerate market adoption and protect pricing power.
Based on the device's established success in other markets and unique position as the only FDA-approved cementless partial knee in the U.S., this could generate meaningful revenue growth for ZBH's knee segment starting in 2025, potentially adding
WARSAW, Ind., Nov. 25, 2024 /PRNewswire/ -- Zimmer Biomet Holdings, Inc. (NYSE and SIX: ZBH), a global medical technology leader, today announced
"Cementless knee replacement procedures are increasingly preferred by surgeons seeking to improve surgical efficiency. The Oxford Cementless Partial Knee is coming into the
Compared to traditional partial knee replacements that use bone cement to secure the implant in place, a cementless approach allows patients' natural bone growth to secure the implant for better long-term fixation.2 The Oxford Cementless Partial Knee features a mobile bearing that can move with the femoral component throughout the entire range of motion to mimic natural knee movement. This design provides better range of motion, a more natural feel and a more stable implant-to-bone fixation for improved long-term implant survival.2,3 The system's tibial and femoral components have a titanium and hydroxyapatite coating to promote bone growth into the implant7. The
"For younger and more active patients, the Oxford Cementless Partial Knee amplifies the benefits of a traditional partial knee replacement by offering knee flexion that resembles natural knee movement, and stronger adhesion of the implant to the bone for better long-term durability," said Adolph V. Lombardi Jr., MD, FACS, President of JIS Orthopedics in
Since its initial launch in
As part of the
Important Safety Information:
The Cementless Oxford Partial Knee System is intended for use in unilateral knee procedures with osteoarthritis or avascular necrosis limited to the medial compartment of the knee. It is intended to be implanted without the application of cement for patients whose clinical condition would benefit from a shorter surgical time compared to the cemented implant. The Oxford Partial Knee is not indicated for use in the lateral compartment or for patients with ligament deficiency, or for use in simultaneous bilateral surgery or planned staged bilateral procedures. Potential risks include, but are not limited to, loosening, dislocation, fracture, wear and infection, any of which can require additional surgery. For a full list of product indications, contraindications and warnings, as well as further information on product IDE data, please see the associated product Information for Use (IFU) and Surgical Technique available at https://labeling.zimmerbiomet.com/
For more information about the Oxford Cementless Partial Knee, visit www.zimmerbiomet.com/oxfordcementless.
About Zimmer Biomet
Zimmer Biomet is a global medical technology leader with a comprehensive portfolio designed to maximize mobility and improve health. We seamlessly transform the patient experience through our innovative products and suite of integrated digital and robotic technologies that leverage data, data analytics and artificial intelligence.
With 90+ years of trusted leadership and proven expertise, Zimmer Biomet is positioned to deliver the highest quality solutions to patients and providers. Our legacy continues to come to life today through our progressive culture of evolution and innovation.
For more information about our product portfolio, our operations in 25+ countries and sales in 100+ countries or about joining our team, visit www.zimmerbiomet.com or follow on LinkedIn at www.linkedin.com/company/zimmerbiomet or X / Twitter at www.twitter.com/zimmerbiomet.
Cautionary Statement Regarding Forward-Looking Statements
This news release contains forward-looking statements within the meaning of the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. Forward-looking statements include, but are not limited to, statements concerning Zimmer Biomet's expectations, plans, prospects, and product and service offerings, including new product launches and potential clinical successes. Such statements are based upon the current beliefs and expectations of management and are subject to significant risks, uncertainties and changes in circumstances that could cause actual outcomes and results to differ materially. For a list and description of some of such risks and uncertainties, see Zimmer Biomet's periodic reports filed with the
*Subject to terms and conditions set forth within the written warranty
References:
- IFU and Surgical Technique for IDE clinical data
- Mohammad, Hasan R., Andrew Judge, and David W. Murray. "A Matched Comparison of Implant and Functional Outcomes of Cemented and Cementless Unicompartmental Knee Replacements: A Study from the National Joint Registry for
England ,Wales ,Northern Ireland and theIsle of Man and the Hospital Episode Statistics Patient Reported Outcome Measures Database." JBJS 106.17 (2024): 1553-1562. - National Joint Registry of England Wales,
Northern Ireland , theIsle of Man andGuernsey . 20th Annual Report 2023 - Pandit, H., et al. "Improved fixation in cementless unicompartmental knee replacement: five-year results of a randomized controlled trial." JBJS 95.15 (2013): 1365-1372.
- Internal Data on File: Sales Data November 2024
- Liddle, A. D., et al. "Patient-reported outcomes after total and unicompartmental knee arthroplasty: a study of 14 076 matched patients from the National Joint Registry for
England andWales ." The bone & joint journal 97.6 (2015): 793-801. - Botterill J, Khatkar H. The role of hydroxyapatite coating in joint replacement surgery - Key considerations. J Clin Orthop Trauma. 2022 Apr 22;29:101874. doi: 10.1016/j.jcot.2022.101874. PMID: 35515345; PMCID: PMC9062319.
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SOURCE Zimmer Biomet Holdings, Inc.
FAQ
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