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FDA 510(k)

BRANEMARK SYSTEM DRILLS AND COUNTERSINKS

K-Number: K925770 · 1993-09-16

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

Device Summary

BRANEMARK SYSTEM DRILLS AND COUNTERSINKS 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 K925770. 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 DRILLS AND COUNTERSINKS?

BRANEMARK SYSTEM DRILLS AND COUNTERSINKS 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 K925770.

When did BRANEMARK SYSTEM DRILLS AND COUNTERSINKS receive FDA 510(k) clearance?

BRANEMARK SYSTEM DRILLS AND COUNTERSINKS received FDA 510(k) clearance on 1993-09-16, under 510(k) number K925770.

Who is the listed applicant for BRANEMARK SYSTEM DRILLS AND COUNTERSINKS?

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 DRILLS AND COUNTERSINKS?

The FDA product code for BRANEMARK SYSTEM DRILLS AND COUNTERSINKS is DZE.

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Other records listing Nobelpharma USA, Inc. as applicant

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Related Devices (Code: DZE)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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