NOBELACTIVE ZIRCONIA ABUTMENT

Abutment, Implant, Dental, Endosseous

NOBEL BIOCARE AB

The following data is part of a premarket notification filed by Nobel Biocare Ab with the FDA for Nobelactive Zirconia Abutment.

Pre-market Notification Details

• Device ID: K072129
• 510k Number: K072129
• Device Name: NOBELACTIVE ZIRCONIA ABUTMENT
• Classification: Abutment, Implant, Dental, Endosseous
• Applicant: NOBEL BIOCARE AB 22715 SAVI RANCH PKWY. Yorba Linda, CA 92887
• Contact: Herbert Crane
• Correspondent: Herbert Crane; NOBEL BIOCARE AB 22715 SAVI RANCH PKWY. Yorba Linda, CA 92887
• Product Code: NHA
• CFR Regulation Number: 872.3630 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2007-08-02
• Decision Date: 2008-02-22
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
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