510(k) K211567 ยท LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
BiMobile Instruments (for BiMobile Dual Mobility System)
| Applicant | Waldemar Link GmbH & Co. KG, Norderstedt, DE |
| Decision | Substantially Equivalent, Jun 3, 2022 |
| Received | May 21, 2021 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K211567
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.