- Oxford® Partial Knee System: Cementless Application Instructions for Use (IFU) 5400000431-US
- Internal Sales Data as of November 2024
- National Joint Registry of England Wales, Northern Ireland, the Isle of Man and Guernsey. 20th Annual Report 2023
- Internal Summary_202100608_GLBLPKRMRKT
- Pandit, H., et al. "Improved fixation in cementless unicompartmental knee replacement: five-year results of a randomized controlled trial." JBJS 95.15 (2013): 1365-1372.
- Stempin R, Kaczmarek W, Stempin K, Dutka J. Midterm Results of Cementless and Cemented Unicondylar Knee Arthroplasty with Mobile Meniscal Bearing: A Prospective Cohort Study. Open Orthop J. 2017 Oct 31;11:1173-1178. doi: 10.2174/1874325001711011173. PMID: 29290853; PMCID: PMC5721307
- Panzram, Benjamin, et al. "Fast return to sports and high level of activity after cementless oxford unicompartmental knee arthroplasty." The Journal of Knee Surgery 34.11 (2021): 1212-1219.
- Panzram, Benjamin, et al. "Cementless unicompartmental knee replacement allows early return to normal activity." BMC Musculoskeletal Disorders 19 (2018): 1-7.


PROVEN.1-3 PREFERRED.4* EFFICIENT.5-6
The proven1-3 Oxford
Cementless Partial Knee, part of the most preferred4*
partial knee system in the world, allows surgeons to be more
efficient5-6 in the O.R. and helps retain healthy anatomy
in patients with Anterior-medial osteoarthritis (AMOA), giving the
best opportunity to get back to what they loved before knee pain.7-8
Oxford Cementless Partial Knee is a Pre-Market Approval (PMA) device,
and the FDA requires anyone who wants to use the implant be certifed
through a training course offered by Zimmer Biomet.
Our training course is an in-depth high-quality course that covers the following:
- Surgical Technique
- Patient Selection
- Differences in Cemented vs. Cementless
- Post-Operative Care Tips
- Oxford Clinical History
- Hands-on Workshop
Important Safety Information: The Oxford Cementless Partial Knee System is indicated for use in unilateral knee procedures with osteoarthritis or avascular necrosis limited to the medial compartment of the knee. It is intended to be implanted without the application of bone cement for patients whose clinical condition would benefit from a shorter surgical time compared to the cemented implant. The Oxford Cementless Partial Knee is not indicated for use in the lateral compartment or for patients with ligament deficiency, or for use in simultaneous bilateral surgery or planned staged bilateral procedures. Potential risks include, but are not limited to, loosening, dislocation, fracture, wear and infection, any of which can require additional surgery. For a full list of product indications, contraindications and warnings, please see the associated product Instructions for Use.
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Disclaimer
All content herein is protected by copyright, trademarks and other intellectual property rights, as applicable, owned by or licensed to Zimmer Biomet or its affiliates unless otherwise indicated, and must not be redistributed, duplicated or disclosed, in whole or in part, without the express written consent of Zimmer Biomet.
Zimmer Biomet does not practice medicine; only a surgeon can answer your questions regarding your individual symptoms, diagnosis and treatment.
Talk to your surgeon about whether joint replacement or another
treatment is right for you and the risks of the procedure, including
the risk of implant wear, loosening or failure, and pain, swelling and
infection.
For printed information on joint replacement, call 1-800-447-5633.
All content herein is protected by copyright, trademarks and other intellectual property rights, as applicable, owned by or licensed to Zimmer Biomet or its affiliates unless otherwise indicated, and must not be redistributed, duplicated or disclosed, in whole or in part, without the express written consent of Zimmer Biomet.
This material is intended for health care professionals. Distribution to any other recipient is prohibited.
For product information, including indications, contraindications, warnings, precautions, potential adverse effects and patient counseling information, see the package insert and information on this website. To obtain a copy of the current Instructions for Use (IFU) for full prescribing and risk information, please call 1-800-348-2759, press 4 for 411 Technical Support.
©2024 Zimmer Biomet
Disclaimer
All content herein is protected by copyright, trademarks and other intellectual property rights, as applicable, owned by or licensed to Zimmer Biomet or its affiliates unless otherwise indicated, and must not be redistributed, duplicated or disclosed, in whole or in part, without the express written consent of Zimmer Biomet.
Zimmer Biomet does not practice medicine; only a surgeon can answer your questions regarding your individual symptoms, diagnosis and treatment.
Talk to your surgeon about whether joint replacement or another
treatment is right for you and the risks of the procedure, including
the risk of implant wear, loosening or failure, and pain, swelling and
infection.
For printed information on joint replacement, call 1-800-447-5633.