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FDA 510(k)

BRANEMARK SYSTEM SCREW TAP

K-Number: K925768 · 1993-09-16

ApplicantNobelpharma USA, Inc.
Decision Date1993-09-16
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BRANEMARK SYSTEM SCREW TAP 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 1993-09-16 under 510(k) number K925768. 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 SCREW TAP?

BRANEMARK SYSTEM SCREW TAP is a medical device that received FDA 510(k) clearance on 1993-09-16. The listed applicant is Nobelpharma USA, Inc.. The 510(k) number is K925768.

When did BRANEMARK SYSTEM SCREW TAP receive FDA 510(k) clearance?

BRANEMARK SYSTEM SCREW TAP received FDA 510(k) clearance on 1993-09-16, under 510(k) number K925768.

Who is the listed applicant for BRANEMARK SYSTEM SCREW TAP?

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 SCREW TAP?

The FDA product code for BRANEMARK SYSTEM SCREW TAP is DZE.

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Other records listing Nobelpharma USA, Inc. as applicant

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Related Devices (Code: 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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