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XENMATRIX SURGICAL GRAFT

K140501 Class II Special
Decision Date
2014-04-28
Sponsor / Applicant
C. R. Bard

Technical Specification

510(k) Submission ID K140501
Product Code FTM
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.3300
Decision Date 2014-04-28
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

XENMATRIX SURGICAL GRAFT received FDA 510(k) clearance under submission number K140501, sponsored by C. R. Bard. 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 2014-04-28.

Classification & Regulation

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