Clearance Summary
NEWFIX SCREW, WIRE AND PIN FIXARION SYSTEM received FDA 510(k) clearance under submission number K101254, sponsored by Tecnologia Y Diseno Industrial, S.A DE C.V. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2010-07-15.
- Submission: K101254
- Applicant / Sponsor: Tecnologia Y Diseno Industrial, S.A DE C.V
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3040
- Decision date: 2010-07-15
Classification & Regulation
This clearance is catalogued under FDA product code HWC and 21 CFR 888.3040, within the Orthopedic review panel as a Class II device.