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FDA 510(k)

BRANEMARK SYSTEM INTERLOCKING ABUTMENT/GOLD CYLIND

K-Number: K925776 · 1994-02-10

ApplicantNobelpharma USA, Inc.
Decision Date1994-02-10
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BRANEMARK SYSTEM INTERLOCKING ABUTMENT/GOLD CYLIND 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 1994-02-10 under 510(k) number K925776. 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 INTERLOCKING ABUTMENT/GOLD CYLIND?

BRANEMARK SYSTEM INTERLOCKING ABUTMENT/GOLD CYLIND is a medical device that received FDA 510(k) clearance on 1994-02-10. The listed applicant is Nobelpharma USA, Inc.. The 510(k) number is K925776.

When did BRANEMARK SYSTEM INTERLOCKING ABUTMENT/GOLD CYLIND receive FDA 510(k) clearance?

BRANEMARK SYSTEM INTERLOCKING ABUTMENT/GOLD CYLIND received FDA 510(k) clearance on 1994-02-10, under 510(k) number K925776.

Who is the listed applicant for BRANEMARK SYSTEM INTERLOCKING ABUTMENT/GOLD CYLIND?

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 INTERLOCKING ABUTMENT/GOLD CYLIND?

The FDA product code for BRANEMARK SYSTEM INTERLOCKING ABUTMENT/GOLD CYLIND is DZE.

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Other records listing Nobelpharma USA, Inc. as applicant

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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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