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WRISTORE FIXATOR

K012294 Class II Traditional
Decision Date
2002-03-04
Sponsor / Applicant
Millennium Medical Technologies, Inc.

Technical Specification

510(k) Submission ID K012294
Product Code KTT
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 2002-03-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WRISTORE FIXATOR received FDA 510(k) clearance under submission number K012294, sponsored by Millennium Medical Technologies, 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 2002-03-04.

Classification & Regulation

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