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FDA 510(k)

BRANEMARK SYSTEM OVOID & U-SHAPED BAR SYSTEM

K-Number: K952886 · 1995-09-18

ApplicantNobelpharma USA, Inc.
Decision Date1995-09-18
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BRANEMARK SYSTEM OVOID & U-SHAPED BAR SYSTEM 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 1995-09-18 under 510(k) number K952886. 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 OVOID & U-SHAPED BAR SYSTEM?

BRANEMARK SYSTEM OVOID & U-SHAPED BAR SYSTEM is a medical device that received FDA 510(k) clearance on 1995-09-18. The listed applicant is Nobelpharma USA, Inc.. The 510(k) number is K952886.

When did BRANEMARK SYSTEM OVOID & U-SHAPED BAR SYSTEM receive FDA 510(k) clearance?

BRANEMARK SYSTEM OVOID & U-SHAPED BAR SYSTEM received FDA 510(k) clearance on 1995-09-18, under 510(k) number K952886.

Who is the listed applicant for BRANEMARK SYSTEM OVOID & U-SHAPED BAR SYSTEM?

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 OVOID & U-SHAPED BAR SYSTEM?

The FDA product code for BRANEMARK SYSTEM OVOID & U-SHAPED BAR SYSTEM is DZE.

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Other records listing Nobelpharma USA, Inc. as applicant

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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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