510(k) K150522 ยท LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
G7 Dual Mobility System
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, May 1, 2015 |
| Received | Mar 2, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150522
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Mar 23, 2023 | Biomet, Inc. G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 110024462 Open, Classified |
LPH | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.