Summary for ARTG Entry:
Johnson & Johnson Medical Pty Ltd T/A Depuy Australia - LCS Complete Porous Coated Femur - Coated
knee femur prosthesis
ARTG entry for
Medical Device Included Class III
Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes
PO Box 134,NORTH RYDE, NSW, 2113
ARTG Start Date
Medical Device Class III
- The inclusion of the kind of device in the ARTG is subject to compliance with all conditions placed or imposed on the ARTG entry. Refer Part 4-5,
Division 2 (Conditions) of the Therapeutic Goods Act 1989 and Part 5, Division 5.2 (Conditions) of the Therapeutic Goods (Medical Devices) Regulations
2002 for relevant information.
- Breaching conditions of the inclusion related to the device of the kind may lead to suspension or cancellation of the ARTG entry; may be a criminal
offence; and civil penalties may apply.
Depuy Orthopaedics Inc
700 Orthopaedic Drive
Warsaw, IN, 46582
United States Of America
1. LCS Complete Porous Coated Femur - Coated knee femur prosthesis
Single Device Product
33745 Coated knee femur prosthesis
LCS Complete Porous Coated Femur is made of cobalt chrome. It articulates with the tibial insert of a knee
joint prosthesis. It is coated with a Porocoat (sintered titanium beads) which improves fixation and stability
by promoting bone ingrowth.
The LCS Complete Porous Femur is the femoral component of a total knee arthroplasty and is intended for
noncemented use in skeletally mature individuals undergoing primary surgery for reconstructing knees
damaged as a result of noninflammatory degenerative joint disease (NIDJD) or either of its composite
diagnoses of osteoarthritis and post-traumatic arthritis pathologies.
Shape Left and Right
No Specific Conditions included on Record
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Produced at 02.12.2017 at 05:01:51 AEDT
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