510(k) K262369 ยท MBI Fastener, Fixation, Nondegradable, Soft Tissue
AIR+ All-Inside Meniscal Repair Device, Curved Up;AIR+ All-Inside Meniscal Repair Device, Curved Down
| Applicant | Stryker Endoscopy, San Jose CA, US |
| Decision | Substantially Equivalent, Jul 30, 2026 |
| Received | Jul 10, 2026 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K262369
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.