510(k) K191259 ยท HRX Arthroscope
Stryker CrossFlow Integrated Arthroscopy Pump
| Applicant | Stryker Corp., San Jose CA, US |
| Decision | Substantially Equivalent, Jul 12, 2019 |
| Received | May 10, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191259
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.