510(k) K091606 ยท NDN Cement, Bone, Vertebroplasty
VERTAPLEX HV (SINGLE PACK AND DUAL PACK)
| Applicant | Stryker Corp., Kalamazoo MI, US |
| Decision | Substantially Equivalent, Oct 23, 2009 |
| Received | Jun 3, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091606
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.