meddevicedb.com FDA Device Reference

PATHWAY CTS 2000 PELVIC FLOOR TRAINING SYSTEM, MODEL PATHWAY CTS 2000

K001515 Class II Traditional
Decision Date
2000-07-31
Sponsor / Applicant
The Prometheus Group

Technical Specification

510(k) Submission ID K001515
Product Code KPI
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5320
Decision Date 2000-07-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PATHWAY CTS 2000 PELVIC FLOOR TRAINING SYSTEM, MODEL PATHWAY CTS 2000 received FDA 510(k) clearance under submission number K001515, sponsored by The Prometheus Group. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2000-07-31.

Classification & Regulation

This clearance is catalogued under FDA product code KPI and 21 CFR 876.5320, within the Gastroenterology, Urology review panel as a Class II device.