510(k) K072118 ยท NDN Cement, Bone, Vertebroplasty
STRYKER VERTAPLEX RADIOPAQUE BONE CEMENT
| Applicant | Stryker Corp., Kalamazoo MI, US |
| Decision | Substantially Equivalent, Dec 7, 2007 |
| Received | Aug 1, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072118
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.