CALCITEK HA-COATED ENDOSSEOUS DENTAL IMPLANT SYSTEMS
K-Number: K960021 · 1996-02-08
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Device Summary
Frequently Asked Questions
What is the CALCITEK HA-COATED ENDOSSEOUS DENTAL IMPLANT SYSTEMS?
CALCITEK HA-COATED ENDOSSEOUS DENTAL IMPLANT SYSTEMS is a medical device that received FDA 510(k) clearance on 1996-02-08. The listed applicant is Calcitek, Inc.. The 510(k) number is K960021.
When did CALCITEK HA-COATED ENDOSSEOUS DENTAL IMPLANT SYSTEMS receive FDA 510(k) clearance?
CALCITEK HA-COATED ENDOSSEOUS DENTAL IMPLANT SYSTEMS received FDA 510(k) clearance on 1996-02-08, under 510(k) number K960021.
Who is the listed applicant for CALCITEK HA-COATED ENDOSSEOUS DENTAL IMPLANT SYSTEMS?
The FDA 510(k) record lists Calcitek, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CALCITEK HA-COATED ENDOSSEOUS DENTAL IMPLANT SYSTEMS?
The FDA product code for CALCITEK HA-COATED ENDOSSEOUS DENTAL IMPLANT SYSTEMS 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 Calcitek, 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
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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