Clearance Summary
Calix Lumbar Spinal Implant System received FDA 510(k) clearance under submission number K170119, sponsored by X-Spine Systems, 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 2017-09-29.
- Submission: K170119
- Applicant / Sponsor: X-Spine Systems, Inc.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3080
- Decision date: 2017-09-29
Classification & Regulation
This clearance is catalogued under FDA product code MAX and 21 CFR 888.3080, within the Orthopedic review panel as a Class II device.