meddevicedb.com FDA Device Reference

NON-WOVEN TRACHEOTOMY SPONGE

K872807 Class I Traditional
Decision Date
1987-08-04
Sponsor / Applicant
American Silk Sutures, Inc.

Technical Specification

510(k) Submission ID K872807
Product Code GDY
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4450
Decision Date 1987-08-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NON-WOVEN TRACHEOTOMY SPONGE received FDA 510(k) clearance under submission number K872807, sponsored by American Silk Sutures, Inc.. 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 1987-08-04.

Classification & Regulation

This clearance is catalogued under FDA product code GDY and 21 CFR 878.4450, within the General, Plastic Surgery review panel as a Class I device.