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

Origin™ TT Stem

K Number: K243029 · Decision Mar 11, 2025
Classifications
1
FEI Numbers
276
Registration Numbers
276
Same Product Code
530
Applicant Total
44
Review Days
165

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
Origin™ TT Stem
K Number
K243029
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3353
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Signature Orthopaedics Pty, Ltd.
Date Received
September 27, 2024
Decision Date
March 11, 2025
Product Code
LZO
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
LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LZO), 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
K251771 Cambridge Partial Knee
K243021 Longboard Revision Hip Stem
K242674 Freedom Posterior Cervical Screws
K242477 Shoulder Soft Tissue Anchors
K243043 Origin™ Cemented Hip 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. →