510(k) K984290 ยท KWI Prosthesis, Elbow, Hemi-, Radial, Polymer
IMPLEX RADIAL HEAD REPLACEMENT SYSTEM
| Applicant | Implex Corp., Allendale NJ, US |
| Decision | Substantially Equivalent, Jun 1, 1999 |
| Received | Dec 1, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K984290
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.