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

AAP K-WIRE, STEINMANN PIN, CERCLAGE WIRE

K Number: K131459 · Decision Oct 17, 2013
Classifications
1
FEI Numbers
184
Registration Numbers
184
Same Product Code
93
Applicant Total
37
Review Days
150

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
AAP K-WIRE, STEINMANN PIN, CERCLAGE WIRE
K Number
K131459
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Aap Implantate AG
Date Received
May 20, 2013
Decision Date
October 17, 2013
Product Code
JDW
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
JDW Pin, Fixation, Threaded

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JDW), ordered by most recent decision date.

View all

Other Clearances by Aap Implantate AG

K Number Device Name
K254253 LOQTEQ® VA Proximal Humerus Plate 3.5
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
Search all 37 clearances from Aap Implantate AG →