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FDA 510(k)

XPI ANGLED ABUTMENTS

K-Number: K090397 · 2009-06-05

ApplicantKeystone Dental, Inc.
Decision Date2009-06-05
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

XPI ANGLED ABUTMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Keystone Dental, Inc.. It received FDA 510(k) clearance on 2009-06-05 under 510(k) number K090397. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the XPI ANGLED ABUTMENTS?

XPI ANGLED ABUTMENTS is a medical device that received FDA 510(k) clearance on 2009-06-05. The listed applicant is Keystone Dental, Inc.. The 510(k) number is K090397.

When did XPI ANGLED ABUTMENTS receive FDA 510(k) clearance?

XPI ANGLED ABUTMENTS received FDA 510(k) clearance on 2009-06-05, under 510(k) number K090397.

Who is the listed applicant for XPI ANGLED ABUTMENTS?

The FDA 510(k) record lists Keystone Dental, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for XPI ANGLED ABUTMENTS?

The FDA product code for XPI ANGLED ABUTMENTS is NHA.

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Other records listing Keystone Dental, Inc. as applicant

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Related Devices (Code: NHA)

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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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