A Prospective, Single-arm, Trial to Determine Contamination Rates When Using an Antibacterial Incise Drape During Orthopedic Surgery

Inclusion Criteria:

* Subject is ≥ 22 years of age on the day of surgery.
* Subject is scheduled to undergo a unilateral primary arthroplasty procedure on a hip or knee.
* Subject is capable of providing informed consent.
* Subject is willing and able to return for all visits.

Exclusion Criteria:

* Subject is pregnant or lactating prior to surgery.\*

  \*Women who have had surgical sterilization by a medically accepted method (e.g., tubal ligation, hysterectomy, or oophorectomy) or are post-menopausal, defined as not having menstruation for \> 12 months will not be required to undergo pregnancy testing
* Subject is scheduled to undergo a lower extremity bilateral arthroplasty procedure.
* Subject had a previous open knee surgery on the study knee or is scheduled to undergo a revision knee arthroplasty.
* Subject has had a previous surgery for revision femoral acetabular osteotomy or total hip arthroplasty on the study hip.
* Subject is scheduled for lower extremity arthroplasty due to trauma.
* Subject was previously diagnosed with septic arthritis or has a history of infection in the joint.
* Subject has taken any antibiotics within 4 weeks before surgery.
* Subject has an allergy or sensitivity to components of the device (e.g., chlorhexidine gluconate or acrylate-based adhesive).
* Subject is currently enrolled in another trial.