Overview
The primary objectives for the registry is to evaluate the overall incidence of serious complications or adverse events for primary implants and replacement devices, and assess the cost and time efficiency for both physicians and patients. The Registry is a multi ASC data collection registry. Data collection will occur at the time of screening, implant, and 2 weeks after implant at the time of wound check.
Eligibility
Inclusion Criteria:
- Physician recommendation to receive the implant in an Ambulatory Surgical Center (ASC)
Exclusion Criteria:
- N/A