meddevicedb.com FDA Device Reference

DASH HIP

K110021 Class II Traditional
Decision Date
2011-10-18
Sponsor / Applicant
Brainlab AG

Technical Specification

510(k) Submission ID K110021
Product Code OLO
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.4560
Decision Date 2011-10-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DASH HIP received FDA 510(k) clearance under submission number K110021, sponsored by Brainlab AG. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2011-10-18.

Classification & Regulation

This clearance is catalogued under FDA product code OLO and 21 CFR 882.4560, within the Neurology review panel as a Class II device.