meddevicedb.com FDA Device Reference

SYSTEC 280 INTEGRATED SUCTION SYSTEM

K791349 Class II Traditional
Decision Date
1979-09-07
Sponsor / Applicant
Stryker Corp.

Technical Specification

510(k) Submission ID K791349
Product Code BTA
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4780
Decision Date 1979-09-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SYSTEC 280 INTEGRATED SUCTION SYSTEM received FDA 510(k) clearance under submission number K791349, 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 1979-09-07.

Classification & Regulation

This clearance is catalogued under FDA product code BTA and 21 CFR 878.4780, within the General, Plastic Surgery review panel as a Class II device.