510(k) K182321 ยท LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
MobileLink Acetabular Cup System
| Applicant | Waldemar Link GmbH & Co. KG, Norderstedt, DE |
| Decision | Substantially Equivalent, May 24, 2019 |
| Received | Aug 27, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182321
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.