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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 the device name listed in this FDA 510(k) record. The listed applicant is Altatec GmbH. It received FDA 510(k) clearance on 2020-09-29 under 510(k) 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. The listed applicant is Altatec GmbH. The 510(k) number is K193401.

When did Altatec GmbH CAMLOG/CONELOG PROGRESSIVE-LINE Implants receive FDA 510(k) clearance?

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

Who is the listed applicant for Altatec GmbH CAMLOG/CONELOG PROGRESSIVE-LINE Implants?

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 Altatec GmbH CAMLOG/CONELOG PROGRESSIVE-LINE Implants?

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

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Other records listing Altatec GmbH as applicant

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Related Devices (Code: DZE)

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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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