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Diplomat® Spinal System

K151704 Class II Traditional
Decision Date
2016-04-13
Sponsor / Applicant
Signus Medizintechnik GmbH

Technical Specification

510(k) Submission ID K151704
Product Code NKB
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3070
Decision Date 2016-04-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Diplomat® Spinal System received FDA 510(k) clearance under submission number K151704, sponsored by Signus Medizintechnik GmbH. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2016-04-13.

Classification & Regulation

This clearance is catalogued under FDA product code NKB and 21 CFR 888.3070, within the Orthopedic review panel as a Class II device.