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KOMET MEDICAL SURGICAL POWER ACCESORIES

K930109 Class II Traditional
Decision Date
1993-08-25
Sponsor / Applicant
Brassler USA

Technical Specification

510(k) Submission ID K930109
Product Code JDX
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.4580
Decision Date 1993-08-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

KOMET MEDICAL SURGICAL POWER ACCESORIES received FDA 510(k) clearance under submission number K930109, sponsored by Brassler USA. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1993-08-25.

Classification & Regulation

This clearance is catalogued under FDA product code JDX and 21 CFR 888.4580, within the Orthopedic review panel as a Class II device.