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FDA 510(k)

PRE-ANGLED ABUTMENTS

K-Number: K912059 · 1992-02-11

ApplicantCore-Vent Corp.
Decision Date1992-02-11
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PRE-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 1992-02-11 under 510(k) number K912059. 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 PRE-ANGLED ABUTMENTS?

PRE-ANGLED ABUTMENTS is a medical device that received FDA 510(k) clearance on 1992-02-11. The listed applicant is Core-Vent Corp.. The 510(k) number is K912059.

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

PRE-ANGLED ABUTMENTS received FDA 510(k) clearance on 1992-02-11, under 510(k) number K912059.

Who is the listed applicant for PRE-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 PRE-ANGLED ABUTMENTS?

The FDA product code for PRE-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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