510(k) K212569 · QHE Shoulder Arthroplasty Implantation System
Materialise Shoulder System, Materialise Shoulder Guide and Models, SurgiCase Shoulder Planner
| Applicant | Materialise NV, Leuven, BE |
| Decision | Substantially Equivalent, Jan 12, 2022 |
| Received | Aug 16, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212569
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.