FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

LOQTEQ® VA Proximal Humerus Plate 3.5

K Number: K254253 · Decision Mar 24, 2026
Classifications
1
FEI Numbers
519
Registration Numbers
519
Same Product Code
1313
Applicant Total
37
Review Days
85

Basic Information

Device Name
LOQTEQ® VA Proximal Humerus Plate 3.5
K Number
K254253
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Aap Implantate AG
Date Received
December 29, 2025
Decision Date
March 24, 2026
Product Code
HRS
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HRS Plate, Fixation, Bone

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Other Clearances by Aap Implantate AG

K Number Device Name
K233008 Cannulated Headless Bone Screws
K230141 LOQTEQ® VA Elbow Plates 2.7/3.5 System
K211582 LOQTEQ Proximal Humerus Plate 3.5 System
K210043 LOQTEQ Distal Lateral Femur Plate 4.5 System
K182818 LOQTEQ VA Calcaneus Plate 3.5
K182785 LOQTEQ VA Foot Plates 2.5
K161696 aap LOQTEQ® Distal Lateral Humerus Plate 2.7/3.5
K161747 LOQTEQ® 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
K161703 LOQTEQ Distal Fibula Plate 3.5, Cancellous Screw 4.0, Washer
K153034 aap LOQTEQ VA Radius Set 2.5
Search all 37 clearances from Aap Implantate AG →