510(k) K820755 ยท KWL Prosthesis, Hip, Hemi-, Femoral, Metal
THE ORIGINAL LEINBACH PLATFORM TOTAL HIP
| Applicant | Allo Pro Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jun 10, 1982 |
| Received | Mar 19, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820755
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.