meddevicedb.com FDA Device Reference

Advantage/Advantage Fit Delivery Device, Lynx Delivery Device, Obtryx Delivery Device (Curved & Halo), Obtryx II Delivery Device (Curved & Halo), Solyx SIS Delivery Device

K172565 Class II Traditional
Decision Date
2017-12-20
Sponsor / Applicant
Boston Scientific Corporation

Technical Specification

510(k) Submission ID K172565
Product Code PWJ
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.4910
Decision Date 2017-12-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Advantage/Advantage Fit Delivery Device, Lynx Delivery Device, Obtryx Delivery Device (Curved & Halo), Obtryx II Delivery Device (Curved & Halo), Solyx SIS Delivery Device received FDA 510(k) clearance under submission number K172565, sponsored by Boston Scientific Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2017-12-20.

Classification & Regulation

This clearance is catalogued under FDA product code PWJ and 21 CFR 884.4910, within the Obstetrics/Gynecology review panel as a Class II device.