510(k) K162103 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Choice Spine Lumbar Spacer System (Sabre, Shark, Hornet, Harpoon), Choice Spine Interbody Fusion System (Harrier), Choice Spine Vertebral Body Replacement System (Hawkeye)
| Applicant | Choicespine, LP, Knoxville TN, US |
| Decision | Substantially Equivalent, Nov 23, 2016 |
| Received | Jul 29, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162103
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.