510(k) K103284 ยท NQW Orthosis, Spine, Plate, Laminoplasty, Metal
LAMINOPLASY PLATING SYSTEM
| Applicant | Aesculap Implant Systems, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Dec 2, 2010 |
| Received | Nov 5, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K103284
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.