510(k) K223538 ยท OWX Mesh, Surgical, Non-Absorbable, Orthopaedics, Reinforcement Of Tendon
Integrity Implant
| Applicant | Anika Therapeutics, Inc., Beford MA, US |
| Decision | Substantially Equivalent, Aug 17, 2023 |
| Received | Nov 23, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223538
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.