510(k) K142112 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
4WEB SPINAL IMPLANT PRODUCTS
| Applicant | 4Web, Inc., Fr. Myers FL, US |
| Decision | Substantially Equivalent, Sep 23, 2014 |
| Received | Aug 4, 2014 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K142112
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.