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FDA 510(k)

LOQTEQ VA Foot Plates 2.5

K-Number: K182785 · 2019-06-19

ApplicantAap Implantate AG
Decision Date2019-06-19
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LOQTEQ VA Foot Plates 2.5 is a medical device manufactured by Aap Implantate AG. It received FDA 510(k) clearance on 2019-06-19 under approval number K182785. 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 VA Foot Plates 2.5?

LOQTEQ VA Foot Plates 2.5 is a medical device that received FDA 510(k) clearance on 2019-06-19. It is manufactured by Aap Implantate AG. The 510(k) number is K182785.

When was LOQTEQ VA Foot Plates 2.5 approved by the FDA?

LOQTEQ VA Foot Plates 2.5 received FDA 510(k) clearance on 2019-06-19, under approval number K182785.

What company makes LOQTEQ VA Foot Plates 2.5?

LOQTEQ VA Foot Plates 2.5 is manufactured by Aap Implantate AG.

What is the FDA product code for LOQTEQ VA Foot Plates 2.5?

The FDA product code for LOQTEQ VA Foot Plates 2.5 is HRS.

Other Devices by Aap Implantate AG

K161696aap LOQTEQ® Distal Lateral Humerus Plate 2.7/3.5 K161747LOQTEQ® VA Distal Tibia Plate System: LOQTEQ® VA Distal Medial Tibia Plate 3.5; LOQTEQ® VA Distal Anterolateral Tibia Plate 3.5; LOQTEQ® VA Distal Fibula Plate 2.7/3.5 K161703LOQTEQ Distal Fibula Plate 3.5, Cancellous Screw 4.0, Washer K153034aap LOQTEQ VA Radius Set 2.5 K182818LOQTEQ VA Calcaneus Plate 3.5 K211582LOQTEQ Proximal Humerus Plate 3.5 System

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Related Devices (Code: HRS)

K163086VLP MINI-MOD 2.0mm Column PlatesSmith & Nephew, Inc. K162829Medline UNITE® Ankle Fracture Plating SystemMedline Industries, Inc. K162974Biomet Microfixation RibFix Blu Thoracic Fixation SystemBiomet Microfixation K163007Biomet Microfixation SternaLock 360 Sternal Closure SystemBiomet Microfixation K161696aap LOQTEQ® Distal Lateral Humerus Plate 2.7/3.5Aap Implantate AG K161747LOQTEQ® VA Distal Tibia Plate System: LOQTEQ® VA Distal Medial Tibia Plate 3.5; LOQTEQ® VA Distal Anterolateral Tibia Plate 3.5; LOQTEQ® VA Distal Fibula Plate 2.7/3.5Aap Implantate AG

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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