510(k) K113154 ยท NDN Cement, Bone, Vertebroplasty
IVAS BALLOON CATHETER
| Applicant | Stryker Corporation, Kalamazoo MI, US |
| Decision | Substantially Equivalent, Jan 24, 2012 |
| Received | Oct 26, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K113154
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.