510(k) K221468 · MAI Fastener, Fixation, Biodegradable, Soft Tissue
Citregen Tendon Interference Screw (TIS), Citrelock Tendon Fixation Device, Citrespline and Citrelock ACL Implants
| Applicant | Acuitive Technologies, Inc., Alendale NJ, US |
| Decision | Substantially Equivalent, Feb 14, 2023 |
| Received | May 20, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221468
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.