meddevicedb.com FDA Device Reference

GORE SEAMGUARD Bioabsorbable Staple Line Reinforcement

K181940 Class II Special
Decision Date
2018-08-17
Sponsor / Applicant
W. L. Gore & Associates, Inc.

Technical Specification

510(k) Submission ID K181940
Product Code OXC
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.3300
Decision Date 2018-08-17
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GORE SEAMGUARD Bioabsorbable Staple Line Reinforcement received FDA 510(k) clearance under submission number K181940, sponsored by W. L. Gore & Associates, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2018-08-17.

Classification & Regulation

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