510(k) K162062 ยท HRX Arthroscope
AVAmax Vertebral Balloon, AVAflex Vertebral Balloon
| Applicant | Stryker Corporation, Kalamazoo MI, US |
| Decision | Substantially Equivalent, Nov 1, 2016 |
| Received | Jul 26, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162062
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.