510(k) K122783 ยท OQG Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented
PLASMAFIT ACETABULAR CUP AND VITELENE INSERT
| Applicant | Aesculap Implant System, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Oct 30, 2013 |
| Received | Sep 11, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122783
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.