meddevicedb.com FDA Device Reference

INTERFACE BONE VOID FILLER

K112857 Class II Traditional
Decision Date
2011-12-13
Sponsor / Applicant
Biostructures, LLC

Technical Specification

510(k) Submission ID K112857
Product Code MQV
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3045
Decision Date 2011-12-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INTERFACE BONE VOID FILLER received FDA 510(k) clearance under submission number K112857, sponsored by Biostructures, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2011-12-13.

Classification & Regulation

This clearance is catalogued under FDA product code MQV and 21 CFR 888.3045, within the Orthopedic review panel as a Class II device.