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ARTHROSCOPY DISP. & REUSABLE SHAVER BLADES, RECHAR

K896196 Class II Traditional
Decision Date
1989-12-01
Sponsor / Applicant
Orthoconcept, Inc.

Technical Specification

510(k) Submission ID K896196
Product Code HRX
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.1100
Decision Date 1989-12-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ARTHROSCOPY DISP. & REUSABLE SHAVER BLADES, RECHAR received FDA 510(k) clearance under submission number K896196, sponsored by Orthoconcept, 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 1989-12-01.

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.