Research Source
The purpose of this study is to evaluate the efficacy on the use of VersaWrap® in surgery of the foot and ankle. VersaWrap is designed to allow tendon gliding and to protect tendon gliding postoperatively
This is a prospective, multi-center, controlled case series evaluating the use of VersaWrap in surgeries of the foot and ankle. Patients identified by the Investigator in his practice as needing surgery for an Achilles primary or elective insertional repair and meeting all the inclusion and none of the exclusion. Patients will consent to participating in the study, prior to any study procedures.
Inclusion Criteria: 1. Patients that require surgery for Achilles primary or elective insertional repair. Note: primary repair must be conducted within 6 weeks of injury. Additional repairs may be conducted during surgery, confirm with study Sponsor prior to enrollment. Insertional repairs due to trauma are not eligible. 2. Able to understand the requirements of the study, provide a written consent, and willing to comply with the study protocol 3. Age ≥18 years and \<90 years at the time of surgery Exclusion Criteria: 1. Investigator determines that the subject is unlikely to comply with th…
VersaWrap is applied to the affected tendon to allow post-operative gliding.
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