FDA 510(k) FDA class 2 Substantially Equivalent 🇦🇺 Australia

Active-V Total Knee System; World Total Knee System

K Number: K253239 · Decision Dec 23, 2025
Classifications
1
FEI Numbers
219
Registration Numbers
219
Same Product Code
142
Applicant Total
44
Review Days
85

Basic Information

Device Name
Active-V Total Knee System; World Total Knee System
K Number
K253239
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3565
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Signature Orthopaedics Pty, Ltd.
Date Received
September 29, 2025
Decision Date
December 23, 2025
Product Code
MBH
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
MBH Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer

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K Number Device Name
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K242674 Freedom Posterior Cervical Screws
K242477 Shoulder Soft Tissue Anchors
K243043 Origin™ Cemented Hip Stem
K243029 Origin™ TT Stem
K243162 World Liner
K240683 Rx Knee System
K241690 Logical Liner; World Liner; World Knee Patella
Search all 44 clearances from Signature Orthopaedics Pty, Ltd. →