510(k) K161190 ยท LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
G7 Dual Mobility System, Active Articulation System
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, May 26, 2016 |
| Received | Apr 27, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K161190
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.