Clearance Summary
STINGRAY CERVICAL CAGE received FDA 510(k) clearance under submission number K122085, sponsored by Omni Surgical, LP Dba Spine360. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2012-10-17.
- Submission: K122085
- Applicant / Sponsor: Omni Surgical, LP Dba Spine360
- Clearance pathway: Abbreviated
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3080
- Decision date: 2012-10-17
Classification & Regulation
This clearance is catalogued under FDA product code ODP and 21 CFR 888.3080, within the Orthopedic review panel as a Class II device.