510(k) K032245 ยท GAT Suture, Nonabsorbable, Synthetic, Polyethylene
ARTHREX FIBERTAPE (TM), 2MM, ARTHREX FIBERTAPE (TM), 3MM, ARTHREX FIBERTAPE (TM), 4MM, MODELS AR-7237, AR-7238, AR-7239
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Unknown, Jan 14, 2004 |
| Received | Jul 22, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032245
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.