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ZIMMER DENTAL HEX-LOCK PREPARED ABUTMENT (STRAIGHT & ANGLED)

K052600 Class II Special
Decision Date
2005-10-13
Sponsor / Applicant
Zimmer Dental, Inc.

Technical Specification

510(k) Submission ID K052600
Product Code NHA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3630
Decision Date 2005-10-13
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ZIMMER DENTAL HEX-LOCK PREPARED ABUTMENT (STRAIGHT & ANGLED) received FDA 510(k) clearance under submission number K052600, sponsored by Zimmer Dental, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2005-10-13.

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.