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CONSENSUS UNIPOLAR HEAD, COCR

K030205 Class II Traditional
Decision Date
2003-04-01
Sponsor / Applicant
Hayes Medical, Inc.

Technical Specification

510(k) Submission ID K030205
Product Code KWL
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3360
Decision Date 2003-04-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CONSENSUS UNIPOLAR HEAD, COCR received FDA 510(k) clearance under submission number K030205, sponsored by Hayes Medical, 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 2003-04-01.

Classification & Regulation

This clearance is catalogued under FDA product code KWL and 21 CFR 888.3360, within the Orthopedic review panel as a Class II device.