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FDA 510(k)

ABUTMENT SELECTION KIT

K-Number: K960639 · 1996-05-14

ApplicantNobelpharma USA, Inc.
Decision Date1996-05-14
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ABUTMENT SELECTION KIT 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 1996-05-14 under 510(k) number K960639. 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 ABUTMENT SELECTION KIT?

ABUTMENT SELECTION KIT is a medical device that received FDA 510(k) clearance on 1996-05-14. The listed applicant is Nobelpharma USA, Inc.. The 510(k) number is K960639.

When did ABUTMENT SELECTION KIT receive FDA 510(k) clearance?

ABUTMENT SELECTION KIT received FDA 510(k) clearance on 1996-05-14, under 510(k) number K960639.

Who is the listed applicant for ABUTMENT SELECTION KIT?

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 ABUTMENT SELECTION KIT?

The FDA product code for ABUTMENT SELECTION KIT 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

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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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