SI-BONE, Inc. Announces $40 Million Debt Re-Financing
SI-BONE, Inc. (Nasdaq: SIBN), a medical device company in California, has successfully re-financed its existing $40 million credit facility. The new five-year term loan, secured through Solar Capital Partners, features an interest rate of 9.40% plus the greater of the 1-month LIBOR Rate or 0.33%. This strategic move will enhance SI-BONE's balance sheet and provide improved operating flexibility. The new loan includes a 36-month interest-only period followed by 24 months of amortization. The refinancing indicates the company's strong operational performance and dedicated team.
- Successfully refinanced $40 million debt with favorable terms.
- New loan provides additional operating flexibility.
- Interest-only period of 36 months enhances financial management.
- Interest rates set at 9.40% plus LIBOR may increase financial burden.
- High interest rate may affect future profitability.
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SANTA CLARA, Calif., June 01, 2020 (GLOBE NEWSWIRE) -- SI-BONE, Inc., (Nasdaq: SIBN), a Silicon Valley-based medical device company dedicated to solving musculoskeletal disorders of the sacropelvic anatomy, announced today that it has re-financed its existing credit facility. Proceeds from the new
SI-BONE’s new term loan bears interest at a rate per annum equal to
The new facility was provided through Solar Capital Partners. Armentum Partners served as financial advisor to SI-BONE on the transaction.
“In order to further strengthen our balance sheet, we have successfully re-financed our
About SI-BONE
SI-BONE is a medical device company that pioneered the iFuse Implant System, a minimally invasive surgical system for fusion of the sacroiliac joint to treat sacroiliac joint dysfunction. The SI joint is believed to be the last major joint with a clinically proven surgical treatment. The iFuse Implant, commercially available since 2009, is believed to be the only SI joint fusion device supported by multiple prospective clinical studies showing improved pain, patient function and quality of life resulting from treatment. There are over 80 peer-reviewed publications supporting the safety, effectiveness, and biomechanical and economic benefits unique to the iFuse Implant (www.si-bone.com/results). This body of evidence has enabled multiple government and private insurance payors to establish coverage of the SI joint fusion procedure exclusively when performed with the iFuse Implant System.
The iFuse Implant System is intended for sacroiliac fusion for conditions including sacroiliac joint dysfunction that is a direct result of sacroiliac joint disruption and degenerative sacroiliitis. This includes conditions whose symptoms began during pregnancy or in the peripartum period and have persisted postpartum for more than 6 months. The iFuse Implant System is also intended for sacroiliac fusion to augment stabilization and immobilization of the sacroiliac joint in skeletally mature patients undergoing sacropelvic fixation as part of a lumbar or thoracolumbar fusion. As well, the iFuse Implant System is intended for sacroiliac fusion in acute, non-acute, and non-traumatic fractures involving the sacroiliac joint. There are potential risks associated with the iFuse Implant System. It may not be appropriate for all patients and all patients may not benefit.
SI-BONE and iFuse Implant System are registered trademarks of SI-BONE, Inc. ©2020 SI-BONE, Inc. All Rights Reserved. 10759
Media Contact:
Joe Powers
jpowers@si-bone.com
669-206-2521
Investor Contacts:
Lynn Lewis or Carrie Mendivil
investors@SI-BONE.com
415-937-5405