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FDA 510(k)

CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR)

K-Number: K152509 · 2016-01-12

ApplicantAltatec GmbH
Decision Date2016-01-12
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR) is a medical device manufactured by Altatec GmbH. It received FDA 510(k) clearance on 2016-01-12 under approval number K152509. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR)?

CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR) is a medical device that received FDA 510(k) clearance on 2016-01-12. It is manufactured by Altatec GmbH. The 510(k) number is K152509.

When was CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR) approved by the FDA?

CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR) received FDA 510(k) clearance on 2016-01-12, under approval number K152509.

What company makes CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR)?

CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR) is manufactured by Altatec GmbH.

What is the FDA product code for CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR)?

The FDA product code for CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR) is NHA.

Related Clinical Trials

NCT07588789 The Aim of the Study Will be Clinically and Radio Graphically Comparison of Two Implant Designs Used to Treat Atrophied Mandible . Implant Design Comparison Will Done for Implant Stability,Peri-implant Soft Tissue Health Changes and Bone Changes .Patients Will be Divided Randomly Into Two Group ACTIVE_NOT_RECRUITING NCT05883202 Effect of the Abutment-Prosthesis Connection on Marginal Bone Loss and Gingival Sealing Around Dental Implants SUSPENDED NCT04695899 Zirconia Implants for Replacement of a Single Tooth ACTIVE_NOT_RECRUITING

Other Devices by Altatec GmbH

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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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