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PREBENT PLATING WITH VIRTUAL SURGICAL PLANNING

K131674 Class II Special
Decision Date
2013-08-08
Sponsor / Applicant
Biomet Microfixation

Technical Specification

510(k) Submission ID K131674
Product Code JEY
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4760
Decision Date 2013-08-08
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PREBENT PLATING WITH VIRTUAL SURGICAL PLANNING received FDA 510(k) clearance under submission number K131674, sponsored by Biomet Microfixation. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2013-08-08.

Classification & Regulation

This clearance is catalogued under FDA product code JEY and 21 CFR 872.4760, within the Dental review panel as a Class II device.