510(k) K231657 · KWT Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented
AGILON® XO Shoulder Replacement System
| Applicant | Implantcast GmbH, Buxtehude, DE |
| Decision | Substantially Equivalent, Feb 16, 2024 |
| Received | Jun 7, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231657
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.