510(k) K831851 ยท KWL Prosthesis, Hip, Hemi-, Femoral, Metal
STRAIGHT STEM FEMORAL HEAD PROSTHESIS
| Applicant | Proteck, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 6, 1983 |
| Received | Jun 9, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831851
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.