Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CAMLOG IMPLANT SYSTEM MODIFIED IMPLANTS AND ABUTMENTS

K-Number: K083496 · 2009-01-30

ApplicantAltatec GmbH
Decision Date2009-01-30
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CAMLOG IMPLANT SYSTEM MODIFIED IMPLANTS AND ABUTMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Altatec GmbH. It received FDA 510(k) clearance on 2009-01-30 under 510(k) number K083496. 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 IMPLANT SYSTEM MODIFIED IMPLANTS AND ABUTMENTS?

CAMLOG IMPLANT SYSTEM MODIFIED IMPLANTS AND ABUTMENTS is a medical device that received FDA 510(k) clearance on 2009-01-30. The listed applicant is Altatec GmbH. The 510(k) number is K083496.

When did CAMLOG IMPLANT SYSTEM MODIFIED IMPLANTS AND ABUTMENTS receive FDA 510(k) clearance?

CAMLOG IMPLANT SYSTEM MODIFIED IMPLANTS AND ABUTMENTS received FDA 510(k) clearance on 2009-01-30, under 510(k) number K083496.

Who is the listed applicant for CAMLOG IMPLANT SYSTEM MODIFIED IMPLANTS AND ABUTMENTS?

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

What is the FDA product code for CAMLOG IMPLANT SYSTEM MODIFIED IMPLANTS AND ABUTMENTS?

The FDA product code for CAMLOG IMPLANT SYSTEM MODIFIED IMPLANTS AND ABUTMENTS 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Altatec GmbH 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.

K193401Altatec GmbH CAMLOG/CONELOG PROGRESSIVE-LINE ImplantsK160784CAM Titanium BlanksK153779Abutment for BridgesK152509CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR)K113779CONELOG IMPLANT SYSTEMK103252CAMLOG VARIO SR ABUTMENTS

View all 11 devices →

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.

↑