LOQTEQ Distal Lateral Femur Plate 4.5 System
K-Number: K210043 · 2021-03-03
Device Summary
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.
Related Clinical Trials
Other Devices by Aap Implantate AG
Related Devices (Code: HRS)
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.