510(k) K964935 ยท KGS Retention Device, Suture
SUTURE LOCK
| Applicant | Smith & Nephew Endoscopy, Inc., Mansfield MA, US |
| Decision | Substantially Equivalent, Feb 25, 1997 |
| Received | Dec 10, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964935
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.