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EDWARDS ORTHOPAEDICS ARTHROSCOPES AND ACCESSORIES

K880205 Class II Traditional
Decision Date
1988-02-04
Sponsor / Applicant
Baxter Healthcare Corp

Technical Specification

510(k) Submission ID K880205
Product Code HRX
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.1100
Decision Date 1988-02-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EDWARDS ORTHOPAEDICS ARTHROSCOPES AND ACCESSORIES received FDA 510(k) clearance under submission number K880205, sponsored by Baxter Healthcare Corp. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1988-02-04.

Classification & Regulation

This clearance is catalogued under FDA product code HRX and 21 CFR 888.1100, within the Orthopedic review panel as a Class II device.