510(k) K883299 ยท KGS Retention Device, Suture
SUTURE RETENTION DEVICE
| Applicant | Edwards Orthopaedics Div., Baxter Healthcare Corp., Santa Ana CA, US |
| Decision | Substantially Equivalent, Aug 23, 1988 |
| Received | Aug 4, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883299
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.