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FDA 510(k)

BRANEMARK SYSTEM GOLD CYLINDERS AND SCREWS

K-Number: K925773 · 1993-04-14

ApplicantNobelpharma USA, Inc.
Decision Date1993-04-14
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BRANEMARK SYSTEM GOLD CYLINDERS AND SCREWS is the device name listed in this FDA 510(k) record. The listed applicant is Nobelpharma USA, Inc.. It received FDA 510(k) clearance on 1993-04-14 under 510(k) number K925773. 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 SYSTEM GOLD CYLINDERS AND SCREWS?

BRANEMARK SYSTEM GOLD CYLINDERS AND SCREWS is a medical device that received FDA 510(k) clearance on 1993-04-14. The listed applicant is Nobelpharma USA, Inc.. The 510(k) number is K925773.

When did BRANEMARK SYSTEM GOLD CYLINDERS AND SCREWS receive FDA 510(k) clearance?

BRANEMARK SYSTEM GOLD CYLINDERS AND SCREWS received FDA 510(k) clearance on 1993-04-14, under 510(k) number K925773.

Who is the listed applicant for BRANEMARK SYSTEM GOLD CYLINDERS AND SCREWS?

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

What is the FDA product code for BRANEMARK SYSTEM GOLD CYLINDERS AND SCREWS?

The FDA product code for BRANEMARK SYSTEM GOLD CYLINDERS AND SCREWS 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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