Clearance Summary
3D-SPINE received FDA 510(k) clearance under submission number K962377, sponsored by Skill Technologies, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1996-09-03.
- Submission: K962377
- Applicant / Sponsor: Skill Technologies, Inc.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class I
- Regulation citation: 21 CFR 888.1500
- Decision date: 1996-09-03
Classification & Regulation
This clearance is catalogued under FDA product code KQX and 21 CFR 888.1500, within the Orthopedic review panel as a Class I device.