510(k) K181999 ยท PHX Shoulder Prosthesis, Reverse Configuration
Integra TITAN Reverse Shoulder System
| Applicant | Integra LifeSciences Corporation, Austin TX, US |
| Decision | Substantially Equivalent, Oct 12, 2018 |
| Received | Jul 26, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181999
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.