FDA 510(k) Applications Submitted by RTI Surgical, Inc
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K230036 | 12/27/2022 | Pre-Sutured Tendon (4561SC / Single Strand); Pre-Sutured Tendon (4564SC / Quadruple Strand ) | RTI Surgical, Inc |
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