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

Cambridge Partial Knee

K Number: K251771 · Decision Dec 16, 2025
Classifications
1
FEI Numbers
159
Registration Numbers
159
Same Product Code
113
Applicant Total
44
Review Days
189

Basic Information

Device Name
Cambridge Partial Knee
K Number
K251771
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3520
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Signature Orthopaedics Pty, Ltd.
Date Received
June 10, 2025
Decision Date
December 16, 2025
Product Code
HSX
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
HSX Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer

Similar 510(k) Clearances

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

View all

Other Clearances by Signature Orthopaedics Pty, Ltd.

K Number Device Name
K252824 Evolve AP Cup, World Finned Cup, World G-Zero Liner and Oddball Femoral Head
K253239 Active-V Total Knee System; World Total Knee System
K243021 Longboard Revision Hip Stem
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. →