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BIOFRAGMENTABLE BOWEL ANASTOMOSIS RING

K881484 Class II Traditional
Decision Date
1988-05-04
Sponsor / Applicant
Davis & Geck, Inc.

Technical Specification

510(k) Submission ID K881484
Product Code GDW
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4750
Decision Date 1988-05-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIOFRAGMENTABLE BOWEL ANASTOMOSIS RING received FDA 510(k) clearance under submission number K881484, 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 1988-05-04.

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.