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SPECTRA-SYSTEM ABUTMENTS 2008

K081101 Class II Traditional
Decision Date
2009-01-14
Sponsor / Applicant
Implant Direct, LLC

Technical Specification

510(k) Submission ID K081101
Product Code NHA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3630
Decision Date 2009-01-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPECTRA-SYSTEM ABUTMENTS 2008 received FDA 510(k) clearance under submission number K081101, sponsored by Implant Direct, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2009-01-14.

Classification & Regulation

This clearance is catalogued under FDA product code NHA and 21 CFR 872.3630, within the Dental review panel as a Class II device.