510(k) K102339 ยท GAT Suture, Nonabsorbable, Synthetic, Polyethylene
CONMED LINVATEC SEQUENT MENISCAL REPAIR DEVICE
| Applicant | Conmed Linvatec, Largo FL, US |
| Decision | Substantially Equivalent, Nov 23, 2010 |
| Received | Aug 18, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102339
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.