ATLANTIS ABUTMENT IN ZIRCONIA FOR NOBEL BIOCARE REPLACE
K-Number: K062277 · 2006-12-20
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Device Summary
Frequently Asked Questions
What is the ATLANTIS ABUTMENT IN ZIRCONIA FOR NOBEL BIOCARE REPLACE?
ATLANTIS ABUTMENT IN ZIRCONIA FOR NOBEL BIOCARE REPLACE is a medical device that received FDA 510(k) clearance on 2006-12-20. The listed applicant is Atlantis Components, Inc.. The 510(k) number is K062277.
When did ATLANTIS ABUTMENT IN ZIRCONIA FOR NOBEL BIOCARE REPLACE receive FDA 510(k) clearance?
ATLANTIS ABUTMENT IN ZIRCONIA FOR NOBEL BIOCARE REPLACE received FDA 510(k) clearance on 2006-12-20, under 510(k) number K062277.
Who is the listed applicant for ATLANTIS ABUTMENT IN ZIRCONIA FOR NOBEL BIOCARE REPLACE?
The FDA 510(k) record lists Atlantis Components, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ATLANTIS ABUTMENT IN ZIRCONIA FOR NOBEL BIOCARE REPLACE?
The FDA product code for ATLANTIS ABUTMENT IN ZIRCONIA FOR NOBEL BIOCARE REPLACE is NHA.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Atlantis Components, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: NHA)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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