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SIGNATURE PLANNER,SIGNATURE GUIDES

K111863 Class II Traditional
Decision Date
2012-06-15
Sponsor / Applicant
Materialise NV

Technical Specification

510(k) Submission ID K111863
Product Code JDI
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3350
Decision Date 2012-06-15
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 K111863, 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 2012-06-15.

Classification & Regulation

This clearance is catalogued under FDA product code JDI and 21 CFR 888.3350, within the Orthopedic review panel as a Class II device.