510(k) K220833 ยท MAI Fastener, Fixation, Biodegradable, Soft Tissue
Citregen Tendon Interference Screw, Citrelock, Citrefix, Citrespline ACL, and Citrelock ACL
| Applicant | Acuitive Technologies, Inc., Alendale NJ, US |
| Decision | Substantially Equivalent, Nov 4, 2022 |
| Received | Mar 22, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220833
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.