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COVAORTHO-NERVE RESORBABLE COLLAGEN MEMBRANE

K103081 Class II Traditional
Decision Date
2012-03-02
Sponsor / Applicant
Biom'Up Sas

Technical Specification

510(k) Submission ID K103081
Product Code JXI
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5275
Decision Date 2012-03-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COVAORTHO-NERVE RESORBABLE COLLAGEN MEMBRANE received FDA 510(k) clearance under submission number K103081, sponsored by Biom'Up Sas. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2012-03-02.

Classification & Regulation

This clearance is catalogued under FDA product code JXI and 21 CFR 882.5275, within the Neurology review panel as a Class II device.