510(k) K896669 ยท LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
WEBER PERMALOCK
| Applicant | Allo Pro Corp., Clearwater FL, US |
| Decision | Substantially Equivalent for Some Indications, Feb 6, 1990 |
| Received | Nov 27, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896669
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.