meddevicedb.com FDA Device Reference

DEMETECH SILK NONABSORBABLE SUTURE

K023029 Class II Traditional
Decision Date
2002-11-25
Sponsor / Applicant
Demetech Corp.

Technical Specification

510(k) Submission ID K023029
Product Code GAP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.5030
Decision Date 2002-11-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DEMETECH SILK NONABSORBABLE SUTURE received FDA 510(k) clearance under submission number K023029, sponsored by Demetech 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 2002-11-25.

Classification & Regulation

This clearance is catalogued under FDA product code GAP and 21 CFR 878.5030, within the General, Plastic Surgery review panel as a Class II device.