CAUTION: USA federal law restricts this device to sale by or on the order of a physician. The ConforMIS Cruciate Retaining Total Knee Replacement System
(iTotal G2) is intended for use only by fully trained physicians. Prior to use of a ConforMIS device, please review the instructions for use and surgical technique for
a complete listing of indications, contraindications, warnings, precautions, and directions for use. MK-02981-AA 10/14
Customized Knee Implants
Potential to improve outcomes and reduce the risk of adverse events
✓
✓
✓
Fewer transfusions
Fewer adverse events at
discharge
Fewer patients discharged
to an acute care facility
REFERENCES
1. Bourne, et al; Patient Satisfaction after Total Knee Arthroplasty. Who is Satisfied and Who is Not? Clinical Orthopaedics and Related Research; 2010,
468: 57-63
2. Culler, Steven. Hospital Outcomes and Cost for Patients Undergoing a Customized Individually Made TKA vs Off-The-Shelf TKA. International Congress
of Joint Replacement Pan-Pacific 2014. Abstract #018A3
One Patient. One Implant.
One in five patients aren't satisfied with the results of their total knee
replacement.
1
ConforMIS patient-specific implants are intended to address known
causes of dissatisfaction while also creating opportunities for efficiency and cost
savings in the healthcare setting.
A recent clinical study evaluating hospital outcomes and costs in total knee
arthroplasty (TKA) showed that
ConforMIS iTotal
®
patients had:
Comparison of key outcomes between off-the-shelf (OTS) and
ConforMIS TKAs for a series of 248 hospitalizations. * indicates
statistical significance
2
0%
10%
20%
30%
40%
50%
OTS All
ConforMIS All
Adverse Events* Acute Care
Facilities*
Transfusion* <3 LOS*
42%
30%
2%
11%
2%
14%
2%
14%
For more information, visit www.patientspecific.com
