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OSTEONICS SPINAL SYSTEM VERSATILE CROSS CONNECTOR

K990922 Class II Traditional
Decision Date
1999-06-02
Sponsor / Applicant
Howmedica Osteonics Corp.

Technical Specification

510(k) Submission ID K990922
Product Code KWP
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3050
Decision Date 1999-06-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OSTEONICS SPINAL SYSTEM VERSATILE CROSS CONNECTOR received FDA 510(k) clearance under submission number K990922, sponsored by Howmedica Osteonics 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 1999-06-02.

Classification & Regulation

This clearance is catalogued under FDA product code KWP and 21 CFR 888.3050, within the Orthopedic review panel as a Class II device.