510(k) K172032 ยท PLR Spinal Vertebral Body Replacement Device - Cervical
Modulift Vertebral Body Replacement (VBR) System
| Applicant | Aesculap Implants Systems, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Nov 20, 2017 |
| Received | Jul 5, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172032
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.