meddevicedb.com FDA Device Reference

SILK, NONABSORBABLE, SURGICAL SUTURES, USP

K001184 Class II Traditional
Decision Date
2000-06-23
Sponsor / Applicant
Cp Medical

Technical Specification

510(k) Submission ID K001184
Product Code GAP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.5030
Decision Date 2000-06-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SILK, NONABSORBABLE, SURGICAL SUTURES, USP received FDA 510(k) clearance under submission number K001184, sponsored by Cp Medical. 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 2000-06-23.

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.