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IO FIX, IO FIX PLUS, CARPALFIX, EXTREMITY MEDICAL SCREW AND WASHER

K121349 Class II Special
Decision Date
2012-07-18
Sponsor / Applicant
Extremity Medical, LLC

Technical Specification

510(k) Submission ID K121349
Product Code HWC
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 2012-07-18
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IO FIX, IO FIX PLUS, CARPALFIX, EXTREMITY MEDICAL SCREW AND WASHER received FDA 510(k) clearance under submission number K121349, sponsored by Extremity Medical, LLC. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2012-07-18.

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.