meddevicedb.com FDA Device Reference

CLAW (5MM/10MM) ATRAUMATIC GRASP/MICRO FORCEPS

K911180 Class I Traditional
Decision Date
1991-03-29
Sponsor / Applicant
Northgate Technologies, Inc.

Technical Specification

510(k) Submission ID K911180
Product Code HTD
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1991-03-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CLAW (5MM/10MM) ATRAUMATIC GRASP/MICRO FORCEPS received FDA 510(k) clearance under submission number K911180, sponsored by Northgate Technologies, 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 1991-03-29.

Classification & Regulation

This clearance is catalogued under FDA product code HTD and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.