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FDA 510(k)

BRANEMARK SYSTEM SINGLE TOOTH ABUTMENTS,INST&COMP.

K-Number: K925767 · 1993-10-20

ApplicantNobelpharma USA, Inc.
Decision Date1993-10-20
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BRANEMARK SYSTEM SINGLE TOOTH ABUTMENTS,INST&COMP. 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 1993-10-20 under 510(k) number K925767. 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 SINGLE TOOTH ABUTMENTS,INST&COMP.?

BRANEMARK SYSTEM SINGLE TOOTH ABUTMENTS,INST&COMP. is a medical device that received FDA 510(k) clearance on 1993-10-20. The listed applicant is Nobelpharma USA, Inc.. The 510(k) number is K925767.

When did BRANEMARK SYSTEM SINGLE TOOTH ABUTMENTS,INST&COMP. receive FDA 510(k) clearance?

BRANEMARK SYSTEM SINGLE TOOTH ABUTMENTS,INST&COMP. received FDA 510(k) clearance on 1993-10-20, under 510(k) number K925767.

Who is the listed applicant for BRANEMARK SYSTEM SINGLE TOOTH ABUTMENTS,INST&COMP.?

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 SINGLE TOOTH ABUTMENTS,INST&COMP.?

The FDA product code for BRANEMARK SYSTEM SINGLE TOOTH ABUTMENTS,INST&COMP. 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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