510(k) K922186 ยท GDW Staple, Implantable
HEM-O-LOK -- MODIFICATION
| Applicant | Linvatec Corp., Research Triangle Pa NC, US |
| Decision | Substantially Equivalent, Aug 6, 1992 |
| Received | Feb 27, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922186
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.