meddevicedb.com FDA Device Reference

Target Detachable Coils

K161429 Class II Special
Decision Date
2016-06-22
Sponsor / Applicant
Stryker Neurovascular

Technical Specification

510(k) Submission ID K161429
Product Code HCG
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5950
Decision Date 2016-06-22
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Target Detachable Coils received FDA 510(k) clearance under submission number K161429, sponsored by Stryker Neurovascular. The device was reviewed via the Special premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2016-06-22.

Classification & Regulation

This clearance is catalogued under FDA product code HCG and 21 CFR 882.5950, within the Neurology review panel as a Class II device.