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GORE BIO-A Tissue Reinforcement

K163217 Class II Traditional
Decision Date
2017-02-10
Sponsor / Applicant
W. L. Gore & Associates, Inc.

Technical Specification

510(k) Submission ID K163217
Product Code OXF
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.3300
Decision Date 2017-02-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GORE BIO-A Tissue Reinforcement received FDA 510(k) clearance under submission number K163217, sponsored by W. L. Gore & Associates, 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 2017-02-10.

Classification & Regulation

This clearance is catalogued under FDA product code OXF and 21 CFR 878.3300, within the General, Plastic Surgery review panel as a Class II device.