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TEMPSPAN CLEAR MATRIX

K120013 Class II Traditional
Decision Date
2012-05-22
Sponsor / Applicant
Pentron Clinical

Technical Specification

510(k) Submission ID K120013
Product Code ELW
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3660
Decision Date 2012-05-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TEMPSPAN CLEAR MATRIX received FDA 510(k) clearance under submission number K120013, sponsored by Pentron Clinical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2012-05-22.

Classification & Regulation

This clearance is catalogued under FDA product code ELW and 21 CFR 872.3660, within the Dental review panel as a Class II device.