meddevicedb.com FDA Device Reference

PROLENE POLYPROPYLENE LIGATING CLIP

K811935 Class II Traditional
Decision Date
1981-09-11
Sponsor / Applicant
ETHICON, Inc.

Technical Specification

510(k) Submission ID K811935
Product Code FZP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4300
Decision Date 1981-09-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PROLENE POLYPROPYLENE LIGATING CLIP received FDA 510(k) clearance under submission number K811935, sponsored by ETHICON, 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 1981-09-11.

Classification & Regulation

This clearance is catalogued under FDA product code FZP and 21 CFR 878.4300, within the General, Plastic Surgery review panel as a Class II device.