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FDA 510(k)

PDQ AND PDQ-TI ABUTMENT

K-Number: K990367 · 1999-04-21

ApplicantVident
Decision Date1999-04-21
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PDQ AND PDQ-TI ABUTMENT is the device name listed in this FDA 510(k) record. The listed applicant is Vident. It received FDA 510(k) clearance on 1999-04-21 under 510(k) number K990367. 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 PDQ AND PDQ-TI ABUTMENT?

PDQ AND PDQ-TI ABUTMENT is a medical device that received FDA 510(k) clearance on 1999-04-21. The listed applicant is Vident. The 510(k) number is K990367.

When did PDQ AND PDQ-TI ABUTMENT receive FDA 510(k) clearance?

PDQ AND PDQ-TI ABUTMENT received FDA 510(k) clearance on 1999-04-21, under 510(k) number K990367.

Who is the listed applicant for PDQ AND PDQ-TI ABUTMENT?

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

What is the FDA product code for PDQ AND PDQ-TI ABUTMENT?

The FDA product code for PDQ AND PDQ-TI ABUTMENT is DZE.

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Other records listing Vident as applicant

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Related Devices (Code: DZE)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261392TriActive Dental Implant SystemParagon Implant Mfg., LLCK260463ZEROS Dental Implant SystemZeros Co., Ltd.K251188UNIQA® Dental Implants SystemUniqa Dental, Ltd.K251232MegaGen Zygoma Dental Implant SystemMegagen Implant Co., Ltd.K250806Dental Implant SystemA.B. Dental Devices , Ltd.K260006INOSS SystemInosys, Inc.

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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