The following data is part of a premarket notification filed by Cutting Edge Spine, Llc with the FDA for Cutting Edge Spine Interbody Fusion Device.
| Device ID | K102957 |
| 510k Number | K102957 |
| Device Name: | CUTTING EDGE SPINE INTERBODY FUSION DEVICE |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | CUTTING EDGE SPINE, LLC 100 E. SOUTH MAIN STREET PO BOX 1458 Matthews, NC 28173 |
| Contact | John Kapitan |
| Correspondent | John Kapitan CUTTING EDGE SPINE, LLC 100 E. SOUTH MAIN STREET PO BOX 1458 Matthews, NC 28173 |
| Product Code | MAX |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-10-05 |
| Decision Date | 2011-04-28 |
| Summary: | summary |