510(k) K161108 ยท KWS Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented
Arthrex VaultLock Glenoid
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Aug 29, 2016 |
| Received | Apr 20, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K161108
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.