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FDA 510(k)

POST AND CORE - THIN FOR THE BASIC DENTAL IMPLANT SYSTEM

K-Number: K022912 · 2002-09-20

Decision Date2002-09-20
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

POST AND CORE - THIN FOR THE BASIC DENTAL IMPLANT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Basic Dental Implant Systems, Inc.. It received FDA 510(k) clearance on 2002-09-20 under 510(k) number K022912. 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 POST AND CORE - THIN FOR THE BASIC DENTAL IMPLANT SYSTEM?

POST AND CORE - THIN FOR THE BASIC DENTAL IMPLANT SYSTEM is a medical device that received FDA 510(k) clearance on 2002-09-20. The listed applicant is Basic Dental Implant Systems, Inc.. The 510(k) number is K022912.

When did POST AND CORE - THIN FOR THE BASIC DENTAL IMPLANT SYSTEM receive FDA 510(k) clearance?

POST AND CORE - THIN FOR THE BASIC DENTAL IMPLANT SYSTEM received FDA 510(k) clearance on 2002-09-20, under 510(k) number K022912.

Who is the listed applicant for POST AND CORE - THIN FOR THE BASIC DENTAL IMPLANT SYSTEM?

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

What is the FDA product code for POST AND CORE - THIN FOR THE BASIC DENTAL IMPLANT SYSTEM?

The FDA product code for POST AND CORE - THIN FOR THE BASIC DENTAL IMPLANT SYSTEM is DZE.

Related Clinical Trials

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.

Other records listing Basic Dental Implant Systems, Inc. as applicant

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.

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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