510(k) K974538 ยท HWC Screw, Fixation, Bone
MENISCAL REPAIR DEVICE
| Applicant | Linvatec Corp., Largo FL, US |
| Decision | Substantially Equivalent, Mar 3, 1998 |
| Received | Dec 3, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K974538
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.