510(k) K781870 ยท KWD Prosthesis, Toe, Hemi-, Phalangeal
IMPLANT, H.P. CONDYLAR
| Applicant | Dow Corning Corp. Healthcare Industries Materials, Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 9, 1979 |
| Received | Nov 3, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K781870
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.