meddevicedb.com FDA Device Reference

PRECISE BARND PI DISPOSABLE SURGICAL STAPLES

K911252 Class II Traditional
Decision Date
1991-07-25
Sponsor / Applicant
3M Medical Products Group

Technical Specification

510(k) Submission ID K911252
Product Code GDW
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4750
Decision Date 1991-07-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PRECISE BARND PI DISPOSABLE SURGICAL STAPLES received FDA 510(k) clearance under submission number K911252, sponsored by 3M Medical Products Group. 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 1991-07-25.

Classification & Regulation

This clearance is catalogued under FDA product code GDW and 21 CFR 878.4750, within the General, Plastic Surgery review panel as a Class II device.