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FDA 510(k)

Altatec GmbH CAMLOG/CONELOG PROGRESSIVE-LINE Implants

K-Number: K193401 · 2020-09-29

ApplicantAltatec GmbH
Decision Date2020-09-29
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Altatec GmbH CAMLOG/CONELOG PROGRESSIVE-LINE Implants is a medical device manufactured by Altatec GmbH. It received FDA 510(k) clearance on 2020-09-29 under approval number K193401. 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 Altatec GmbH CAMLOG/CONELOG PROGRESSIVE-LINE Implants?

Altatec GmbH CAMLOG/CONELOG PROGRESSIVE-LINE Implants is a medical device that received FDA 510(k) clearance on 2020-09-29. It is manufactured by Altatec GmbH. The 510(k) number is K193401.

When was Altatec GmbH CAMLOG/CONELOG PROGRESSIVE-LINE Implants approved by the FDA?

Altatec GmbH CAMLOG/CONELOG PROGRESSIVE-LINE Implants received FDA 510(k) clearance on 2020-09-29, under approval number K193401.

What company makes Altatec GmbH CAMLOG/CONELOG PROGRESSIVE-LINE Implants?

Altatec GmbH CAMLOG/CONELOG PROGRESSIVE-LINE Implants is manufactured by Altatec GmbH.

What is the FDA product code for Altatec GmbH CAMLOG/CONELOG PROGRESSIVE-LINE Implants?

The FDA product code for Altatec GmbH CAMLOG/CONELOG PROGRESSIVE-LINE Implants is DZE.

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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