Clearance Summary
MIS Z-Pedicle Screw System received FDA 510(k) clearance under submission number K143200, sponsored by Z-Medical GmbH & Co. KG. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2015-02-03.
- Submission: K143200
- Applicant / Sponsor: Z-Medical GmbH & Co. KG
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3070
- Decision date: 2015-02-03
Classification & Regulation
This clearance is catalogued under FDA product code NKB and 21 CFR 888.3070, within the Orthopedic review panel as a Class II device.