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

TriVerse Total Knee Replacement System

K Number: K222380 · Decision Oct 4, 2022
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
910
Applicant Total
44
Review Days
60

Basic Information

Device Name
TriVerse Total Knee Replacement System
K Number
K222380
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3560
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Signature Orthopaedics Pty, Ltd.
Date Received
August 5, 2022
Decision Date
October 4, 2022
Product Code
JWH
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
JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

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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
K251771 Cambridge Partial Knee
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
Search all 44 clearances from Signature Orthopaedics Pty, Ltd. →