meddevicedb.com FDA Device Reference

3M PRECISE BRAND INTERNAL SURGICAL STAPLES

K921051 Class II Traditional
Decision Date
1992-07-16
Sponsor / Applicant
3M Health Care, Ltd.

Technical Specification

510(k) Submission ID K921051
Product Code GDW
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4750
Decision Date 1992-07-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

3M PRECISE BRAND INTERNAL SURGICAL STAPLES received FDA 510(k) clearance under submission number K921051, sponsored by 3M Health Care, Ltd.. 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 1992-07-16.

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.