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KneeWell (Prod 200219 T202002
Manufacturer Info:
Kneewell, LLC
6024 Blue Circle Drive
Minnetonka, MN 55343
USA
Phone:
952/546-5334
Fax:
952/546-2657
Website:
www.kneewell.com
About KneeWell (Prod 200219 T202002
Device designed to assist patients with flexion contractures following knee surgery
- Intensity of the load controllable by the patient, which minimizes pain and encourages compliance
- Classified by Medicare as a low-load, prolonged-stretchg device
- Has a HCPCS code for reimbursement for patient use
- Approved on the basis of a capped rental allowing for 13 months of use, but most patients require no more than 3 months
- Easy for patients to understand
- Easily transported
- FDA registered
- Patented
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OrthopaedicLIST.com is a list of products and services. Every effort is made to keep this listing as accurate and current as possible. Companies and individuals are encouraged to notify us of errors and omissions. We will respond to such messages of correction in a timely fashion, as our workload permits.
We are non-judgmental of products listed. We are not in the business of evaluating products. We have not evaluated these products. We make no representations as to the quality, effectiveness, suitability or appropriateness of any of the products listed.
As an important component of the service function of OrthopaedicLIST.com, some products continue to be listed that are no longer manufactured and may not be available. We will identify them as such when possible. This allows users to find special instruments and/or components for removal, modification, and/or revision of those products.