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LOCKING BONE SCREW MODEL HCQ04, HCZ04

K100721 Class II Traditional
Decision Date
2010-11-23
Sponsor / Applicant
Changzhou Orthmar Medical Instrument Co., Ltd.

Technical Specification

510(k) Submission ID K100721
Product Code HWC
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 2010-11-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LOCKING BONE SCREW MODEL HCQ04, HCZ04 received FDA 510(k) clearance under submission number K100721, sponsored by Changzhou Orthmar Medical Instrument Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2010-11-23.

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.