PATHWAY STM-10 PELVIC FLOOR STIMULATOR— 510(k) K030039
Substantially EquivalentThe Prometheus Group
FDA 510(k) clearance K030039 for PATHWAY STM-10 PELVIC FLOOR STIMULATOR, Substantially Equivalent on 2003-05-23. Applicant: The Prometheus Group.
Clearance details
- Applicant
- The Prometheus Group
- Product code
- Code KPI
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Duxbury, MA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.