510(k) K202153 ยท MBI Fastener, Fixation, Nondegradable, Soft Tissue
Responsive Arthroscopy Suture Anchor System
| Applicant | Responsive Arthroscopy, LLC, Minneapolis MN, US |
| Decision | Substantially Equivalent, Sep 9, 2020 |
| Received | Aug 3, 2020 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K202153
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.