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SURGI-WRAP MAST BIORESORBABLE SHEET

K061473 Class II Traditional
Decision Date
2006-09-21
Sponsor / Applicant
Mast Biosurgery USA, Inc.

Technical Specification

510(k) Submission ID K061473
Product Code FTL
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.3300
Decision Date 2006-09-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SURGI-WRAP MAST BIORESORBABLE SHEET received FDA 510(k) clearance under submission number K061473, sponsored by Mast Biosurgery USA, 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 2006-09-21.

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.