meddevicedb.com FDA Device Reference

NON-ABSORBABLE SILK SUTURE

K071111 Class II Traditional
Decision Date
2007-07-17
Sponsor / Applicant
Arrow Intl., Inc.

Technical Specification

510(k) Submission ID K071111
Product Code GAP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.5030
Decision Date 2007-07-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NON-ABSORBABLE SILK SUTURE received FDA 510(k) clearance under submission number K071111, sponsored by Arrow 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 2007-07-17.

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.