meddevicedb.com FDA Device Reference

REGULAR AND WIDE SKIN STAPLES

K760734 Class I Traditional
Decision Date
1976-11-03
Sponsor / Applicant
ETHICON, Inc.

Technical Specification

510(k) Submission ID K760734
Product Code GDT
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4760
Decision Date 1976-11-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

REGULAR AND WIDE SKIN STAPLES received FDA 510(k) clearance under submission number K760734, sponsored by ETHICON, 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 1976-11-03.

Classification & Regulation

This clearance is catalogued under FDA product code GDT and 21 CFR 878.4760, within the General, Plastic Surgery review panel as a Class I device.