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FDA 510(k)

BRANEMARK NOVUM

K-Number: K000018 · 2000-03-30

ApplicantNobel Biocare Uas, Inc.
Decision Date2000-03-30
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BRANEMARK NOVUM 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 2000-03-30 under 510(k) number K000018. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRANEMARK NOVUM?

BRANEMARK NOVUM is a medical device that received FDA 510(k) clearance on 2000-03-30. The listed applicant is Nobel Biocare Uas, Inc.. The 510(k) number is K000018.

When did BRANEMARK NOVUM receive FDA 510(k) clearance?

BRANEMARK NOVUM received FDA 510(k) clearance on 2000-03-30, under 510(k) number K000018.

Who is the listed applicant for BRANEMARK NOVUM?

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 BRANEMARK NOVUM?

The FDA product code for BRANEMARK NOVUM is DZE.

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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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