meddevicedb.com FDA Device Reference

SURGICAL INSTRUMENTS AND ACCESSORIES

K942956 Class I Traditional
Decision Date
1994-09-23
Sponsor / Applicant
Stryker Corp.

Technical Specification

510(k) Submission ID K942956
Product Code HWE
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4820
Decision Date 1994-09-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SURGICAL INSTRUMENTS AND ACCESSORIES received FDA 510(k) clearance under submission number K942956, sponsored by Stryker Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1994-09-23.

Classification & Regulation

This clearance is catalogued under FDA product code HWE and 21 CFR 878.4820, within the General, Plastic Surgery review panel as a Class I device.