510(k) K120044 ยท KWS Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented
ARTHREX UNIVERSII XL GLENOID-PEGGED, ARTHREX UNIVERS II XL GLENOID-KEELED
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Mar 8, 2012 |
| Received | Jan 5, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K120044
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.