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FDA 510(k)

TSIR ANGLED ABUTMENTS

K-Number: K910585 · 1991-10-04

ApplicantCore-Vent Corp.
Decision Date1991-10-04
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TSIR ANGLED ABUTMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Core-Vent Corp.. It received FDA 510(k) clearance on 1991-10-04 under 510(k) number K910585. 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 TSIR ANGLED ABUTMENTS?

TSIR ANGLED ABUTMENTS is a medical device that received FDA 510(k) clearance on 1991-10-04. The listed applicant is Core-Vent Corp.. The 510(k) number is K910585.

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

TSIR ANGLED ABUTMENTS received FDA 510(k) clearance on 1991-10-04, under 510(k) number K910585.

Who is the listed applicant for TSIR ANGLED ABUTMENTS?

The FDA 510(k) record lists Core-Vent Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TSIR ANGLED ABUTMENTS?

The FDA product code for TSIR ANGLED ABUTMENTS 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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