510(k) K812053 ยท KXE Prosthesis, Wrist, Hemi-, Ulnar
SILASTIC HEMI WRIST IMPLANT H.P. (RAD.)
| Applicant | Dow Corning Corp. Healthcare Industries Materials, Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 18, 1981 |
| Received | Jul 21, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K812053
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.