510(k) K173411 ยท PHX Shoulder Prosthesis, Reverse Configuration
Comprehensive Segmental Revision System (SRS)
| Applicant | Biomet Manufacturing Corp, Warsaw IN, US |
| Decision | Substantially Equivalent, Feb 8, 2018 |
| Received | Nov 1, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173411
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.