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ExactechGPS Total Shoulder Application, Equinoxe Planning Software

K162567 Class II Traditional
Decision Date
2017-04-05
Sponsor / Applicant
Blue Ortho

Technical Specification

510(k) Submission ID K162567
Product Code OLO
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.4560
Decision Date 2017-04-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ExactechGPS Total Shoulder Application, Equinoxe Planning Software received FDA 510(k) clearance under submission number K162567, sponsored by Blue Ortho. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2017-04-05.

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.