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NEXT GENERATION RODDING SYSTEM

K992784 Class II Traditional
Decision Date
1999-10-27
Sponsor / Applicant
United States Surgical, A Division of Tyco Healthc

Technical Specification

510(k) Submission ID K992784
Product Code KWQ
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3060
Decision Date 1999-10-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NEXT GENERATION RODDING SYSTEM received FDA 510(k) clearance under submission number K992784, sponsored by United States Surgical, A Division of Tyco Healthc. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1999-10-27.

Classification & Regulation

This clearance is catalogued under FDA product code KWQ and 21 CFR 888.3060, within the Orthopedic review panel as a Class II device.