510(k) K171657 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ShurFit 2C Lumbar Interbody Fusion System
| Applicant | Precision Spine, Inc., Pear MS, US |
| Decision | Substantially Equivalent, Aug 11, 2017 |
| Received | Jun 5, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171657
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.