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MICROSURGICAL INSTRUMENTS

K911300 Class II Traditional
Decision Date
1991-04-05
Sponsor / Applicant
Danek Medical, Inc.

Technical Specification

510(k) Submission ID K911300
Product Code HRX
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.1100
Decision Date 1991-04-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MICROSURGICAL INSTRUMENTS received FDA 510(k) clearance under submission number K911300, sponsored by Danek 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 1991-04-05.

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.