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FDA 510(k)

LOQTEQ Distal Lateral Femur Plate 4.5 System

K-Number: K210043 · 2021-03-03

Decision Date2021-03-03
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LOQTEQ Distal Lateral Femur Plate 4.5 System is a medical device manufactured by Aap Implantate AG. It received FDA 510(k) clearance on 2021-03-03 under approval number K210043. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LOQTEQ Distal Lateral Femur Plate 4.5 System?

LOQTEQ Distal Lateral Femur Plate 4.5 System is a medical device that received FDA 510(k) clearance on 2021-03-03. It is manufactured by Aap Implantate AG. The 510(k) number is K210043.

When was LOQTEQ Distal Lateral Femur Plate 4.5 System approved by the FDA?

LOQTEQ Distal Lateral Femur Plate 4.5 System received FDA 510(k) clearance on 2021-03-03, under approval number K210043.

What company makes LOQTEQ Distal Lateral Femur Plate 4.5 System?

LOQTEQ Distal Lateral Femur Plate 4.5 System is manufactured by Aap Implantate AG.

What is the FDA product code for LOQTEQ Distal Lateral Femur Plate 4.5 System?

The FDA product code for LOQTEQ Distal Lateral Femur Plate 4.5 System is HRS.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.