510(k) K133053 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
MILESTONE SPINAL SYSTEM
| Applicant | Weigao Orthopaedic Device Co., Ltd., Shanghai, CN |
| Decision | Substantially Equivalent, Jul 15, 2014 |
| Received | Sep 27, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133053
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.