meddevicedb.com FDA Device Reference

POLYPROPYLENE

K993997 Class II Traditional
Decision Date
2000-02-04
Sponsor / Applicant
Trading Consultants and Distributors Intl., Inc.

Technical Specification

510(k) Submission ID K993997
Product Code GAW
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.5010
Decision Date 2000-02-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POLYPROPYLENE received FDA 510(k) clearance under submission number K993997, sponsored by Trading Consultants and Distributors Intl., 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 2000-02-04.

Classification & Regulation

This clearance is catalogued under FDA product code GAW and 21 CFR 878.5010, within the General, Plastic Surgery review panel as a Class II device.