510(k) K173347 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
STALIF C FLX, STALIF M FLX, STALIF L FLX and STALIF Lateral-Oblique FLX, ACTILIF C FLX, ACTILIF M FLX, ACTILIF L FLX and ACTILIF Lateral-Oblique FLX
| Applicant | Centinel Spine, Inc., West Chester PA, US |
| Decision | Substantially Equivalent, May 8, 2018 |
| Received | Oct 25, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173347
No recall in the FDA data names this 510(k).
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