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SIGNATURE PLANNER / SIGNATURE GUIDES

K110415 Class II Traditional
Decision Date
2011-05-16
Sponsor / Applicant
Materialise NV

Technical Specification

510(k) Submission ID K110415
Product Code HRY
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3530
Decision Date 2011-05-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SIGNATURE PLANNER / SIGNATURE GUIDES received FDA 510(k) clearance under submission number K110415, sponsored by Materialise NV. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2011-05-16.

Classification & Regulation

This clearance is catalogued under FDA product code HRY and 21 CFR 888.3530, within the Orthopedic review panel as a Class II device.