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SURGICAL PATCH, SURGICAL MEMBRANE, SURGICAL MESH

K961440 Class II Traditional
Decision Date
1996-05-31
Sponsor / Applicant
Fusion Medical Technologies, Inc.

Technical Specification

510(k) Submission ID K961440
Product Code FTL
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.3300
Decision Date 1996-05-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SURGICAL PATCH, SURGICAL MEMBRANE, SURGICAL MESH received FDA 510(k) clearance under submission number K961440, sponsored by Fusion Medical Technologies, 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 1996-05-31.

Classification & Regulation

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