meddevicedb.com FDA Device Reference

NEEDLES AND SUTURES, SILK & NYLON

K760158 Class II Traditional
Decision Date
1976-08-19
Sponsor / Applicant
Alcon Laboratories

Technical Specification

510(k) Submission ID K760158
Product Code GAP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.5030
Decision Date 1976-08-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NEEDLES AND SUTURES, SILK & NYLON received FDA 510(k) clearance under submission number K760158, sponsored by Alcon Laboratories. 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 1976-08-19.

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.