510(k) K153107 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Choice Spine Lumbar Spacer System (Sabre, Shark, Hornet, Harpoon), Choice Spine VEO Lateral Access & Interbody Fusion System, Choice Spine Interbody Fusion System
| Applicant | Choicespine, LP, Knoxville TN, US |
| Decision | Substantially Equivalent, May 19, 2016 |
| Received | Oct 27, 2015 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K153107
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.