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MACROPORE SURGI-WRAP MAST BIORESORBABLE SHEET

K031955 Class II Traditional
Decision Date
2003-09-22
Sponsor / Applicant
Macropore Biosurgery, Inc.

Technical Specification

510(k) Submission ID K031955
Product Code FTL
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.3300
Decision Date 2003-09-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MACROPORE SURGI-WRAP MAST BIORESORBABLE SHEET received FDA 510(k) clearance under submission number K031955, sponsored by Macropore Biosurgery, 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 2003-09-22.

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.