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Actis Total Hip System 2 Year Follow-up

Principal Investigator

David Jevsevar

Study Number

F16103

Summary

Two-year (2 year) information regarding the performance of the commercially available Actis(tm) Total Hip System in order to obtain and evaluate the clinical outcomes on a series of cementless primary total hip arthroplasty (THA) and hemi-hip arthroplasty procedures using clinical, radiographic and device and procedure related adverse event assessments.

Phase

N/A

Contact

Peter DePalo Sr.

Available at the following location(s)

  • Lebanon

View more details at ClinicalTrials.gov

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