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FDA 510(k)

CAMLOG CYLINDER IMPLANT SYSTEM

K-Number: K000065 · 2000-01-28

ApplicantAltatec Biotechnologies
Decision Date2000-01-28
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CAMLOG CYLINDER IMPLANT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Altatec Biotechnologies. It received FDA 510(k) clearance on 2000-01-28 under 510(k) number K000065. 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 CAMLOG CYLINDER IMPLANT SYSTEM?

CAMLOG CYLINDER IMPLANT SYSTEM is a medical device that received FDA 510(k) clearance on 2000-01-28. The listed applicant is Altatec Biotechnologies. The 510(k) number is K000065.

When did CAMLOG CYLINDER IMPLANT SYSTEM receive FDA 510(k) clearance?

CAMLOG CYLINDER IMPLANT SYSTEM received FDA 510(k) clearance on 2000-01-28, under 510(k) number K000065.

Who is the listed applicant for CAMLOG CYLINDER IMPLANT SYSTEM?

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

What is the FDA product code for CAMLOG CYLINDER IMPLANT SYSTEM?

The FDA product code for CAMLOG CYLINDER 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.

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Other records listing Altatec Biotechnologies 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.

K032448ALTATEC CERAMIC ABUTMENTK000099CAMLOG SCREW IMPLANT SYSTEMK000100CAMLOG ROOTFORM IMPLANT SYSTEM

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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