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FDA 510(k)

NOBEL BIOCARE CENTRIC POST, MODELS 31234, 31235 AND 31236

K-Number: K033724 · 2004-02-23

ApplicantNobel Biocare Uas, Inc.
Decision Date2004-02-23
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

NOBEL BIOCARE CENTRIC POST, MODELS 31234, 31235 AND 31236 is the device name listed in this FDA 510(k) record. The listed applicant is Nobel Biocare Uas, Inc.. It received FDA 510(k) clearance on 2004-02-23 under 510(k) number K033724. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOBEL BIOCARE CENTRIC POST, MODELS 31234, 31235 AND 31236?

NOBEL BIOCARE CENTRIC POST, MODELS 31234, 31235 AND 31236 is a medical device that received FDA 510(k) clearance on 2004-02-23. The listed applicant is Nobel Biocare Uas, Inc.. The 510(k) number is K033724.

When did NOBEL BIOCARE CENTRIC POST, MODELS 31234, 31235 AND 31236 receive FDA 510(k) clearance?

NOBEL BIOCARE CENTRIC POST, MODELS 31234, 31235 AND 31236 received FDA 510(k) clearance on 2004-02-23, under 510(k) number K033724.

Who is the listed applicant for NOBEL BIOCARE CENTRIC POST, MODELS 31234, 31235 AND 31236?

The FDA 510(k) record lists Nobel Biocare Uas, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NOBEL BIOCARE CENTRIC POST, MODELS 31234, 31235 AND 31236?

The FDA product code for NOBEL BIOCARE CENTRIC POST, MODELS 31234, 31235 AND 31236 is NHA.

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Other records listing Nobel Biocare Uas, Inc. as applicant

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K050444NOBELREPLACE ADAPTER, MODEL 32412K042658PROCERA ABUTMENT BRANEMARK, MODELS 10-4001, 10-4004, 10-5001, 10-5004, 10-6001, 10-6004K041661NOBEL BIOCARE ENDOSSEOUS IMPLANTSK041876NOBELDIRECT OD IMPLANTK041312NOBELRONDO DENTAL CERAMIC-ALUMINAK041275PROCERA ABUTMENT OCTAGON

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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.

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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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