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 |