510(k) K170676 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
HD Lumbar Interbody System
| Applicant | Hd Lifesciences, LLC, Stoneham MA, US |
| Decision | Substantially Equivalent, Jul 13, 2017 |
| Received | Mar 6, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170676
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.