510(k) K162800 ยท KWS Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented
BLUEPRINT Patient Specific Instrumentation
| Applicant | Tornier S.A.S., Montbonnot-Saint-Martin, FR |
| Decision | Substantially Equivalent, Feb 22, 2017 |
| Received | Oct 5, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162800
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.