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FDA 510(k)

CAMLOG LOGFIT PROSTHETIC SYSTEM

K-Number: K071213 · 2007-08-10

ApplicantAltatec GmbH
Decision Date2007-08-10
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CAMLOG LOGFIT PROSTHETIC SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Altatec GmbH. It received FDA 510(k) clearance on 2007-08-10 under 510(k) number K071213. 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 LOGFIT PROSTHETIC SYSTEM?

CAMLOG LOGFIT PROSTHETIC SYSTEM is a medical device that received FDA 510(k) clearance on 2007-08-10. The listed applicant is Altatec GmbH. The 510(k) number is K071213.

When did CAMLOG LOGFIT PROSTHETIC SYSTEM receive FDA 510(k) clearance?

CAMLOG LOGFIT PROSTHETIC SYSTEM received FDA 510(k) clearance on 2007-08-10, under 510(k) number K071213.

Who is the listed applicant for CAMLOG LOGFIT PROSTHETIC SYSTEM?

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 LOGFIT PROSTHETIC SYSTEM?

The FDA product code for CAMLOG LOGFIT PROSTHETIC SYSTEM is NHA.

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Other records listing Altatec GmbH as applicant

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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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