510(k) K071375 ยท NDN Cement, Bone, Vertebroplasty
MESH FENESTRATED INTRODUCER NEEDLE (MESH INTRODUCER NEEDLE)
| Applicant | Disc-O-Tech Medical Technologies, Ltd., Washington DC, US |
| Decision | Substantially Equivalent, Dec 21, 2007 |
| Received | May 16, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071375
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.