NEXUS 3

Cement, Dental

KERR CORPORATION

The following data is part of a premarket notification filed by Kerr Corporation with the FDA for Nexus 3.

Pre-market Notification Details

• Device ID: K062519
• 510k Number: K062519
• Device Name: NEXUS 3
• Classification: Cement, Dental
• Applicant: KERR CORPORATION 100 BAYVIEW CIRCLE STE 6000 Newport Beach, CA 92660
• Contact: Colleen Boswell
• Correspondent: Colleen Boswell; KERR CORPORATION 100 BAYVIEW CIRCLE STE 6000 Newport Beach, CA 92660
• Product Code: EMA
• CFR Regulation Number: 872.3275 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2006-08-28
• Decision Date: 2006-10-19
• Summary: summary