510(k) K130402 ยท NDN Cement, Bone, Vertebroplasty
SPIDER SYSTEM KOLIBRI CEMENT NEEDLE
| Applicant | Sintea Plustek, LLC, Apple Valley MN, US |
| Decision | Substantially Equivalent, Apr 1, 2013 |
| Received | Feb 19, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K130402
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.