meddevicedb.com FDA Device Reference

FIXIT Threaded Anchor System

K170868 Class II Traditional
Decision Date
2017-11-30
Sponsor / Applicant
S.B.M Sas Science For Bio Materials

Technical Specification

510(k) Submission ID K170868
Product Code MAI
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 2017-11-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FIXIT Threaded Anchor System received FDA 510(k) clearance under submission number K170868, sponsored by S.B.M Sas Science For Bio Materials. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2017-11-30.

Classification & Regulation

This clearance is catalogued under FDA product code MAI and 21 CFR 888.3030, within the Orthopedic review panel as a Class II device.