meddevicedb.com FDA Device Reference

DAVIS & GECK VALTRAC(R) BIOFRAG ANASTOMOSIS RING

K913411 Class II Traditional
Decision Date
1991-09-06
Sponsor / Applicant
Davis & Geck, Inc.

Technical Specification

510(k) Submission ID K913411
Product Code GDW
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4750
Decision Date 1991-09-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DAVIS & GECK VALTRAC(R) BIOFRAG ANASTOMOSIS RING received FDA 510(k) clearance under submission number K913411, sponsored by Davis & Geck, 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 1991-09-06.

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.