510(k) K181752 ยท HRX Arthroscope
Stryker iVAS Elite Inflatable Vertebral Augmentation System (Stryker iVAS Elite Balloon Catheter)
| Applicant | Stryker Corporation, Kalamazoo MI, US |
| Decision | Substantially Equivalent, Dec 21, 2018 |
| Received | Jul 2, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181752
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.