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 |