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FDA 510(k)

ANGLED ABUTMENT

K-Number: K962647 · 1996-10-07

ApplicantStraumann USA
Decision Date1996-10-07
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ANGLED ABUTMENT is the device name listed in this FDA 510(k) record. The listed applicant is Straumann USA. It received FDA 510(k) clearance on 1996-10-07 under 510(k) number K962647. 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 ANGLED ABUTMENT?

ANGLED ABUTMENT is a medical device that received FDA 510(k) clearance on 1996-10-07. The listed applicant is Straumann USA. The 510(k) number is K962647.

When did ANGLED ABUTMENT receive FDA 510(k) clearance?

ANGLED ABUTMENT received FDA 510(k) clearance on 1996-10-07, under 510(k) number K962647.

Who is the listed applicant for ANGLED ABUTMENT?

The FDA 510(k) record lists Straumann USA as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANGLED ABUTMENT?

The FDA product code for ANGLED ABUTMENT is DZE.

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Related Devices (Code: 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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