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FDA 510(k)

VSP System

K-Number: K192192 · 2020-02-26

Applicant3D Systems
Decision Date2020-02-26
Product CodeDZJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VSP System is a medical device manufactured by 3D Systems. It received FDA 510(k) clearance on 2020-02-26 under approval number K192192. The device is classified under product code DZJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VSP System?

VSP System is a medical device that received FDA 510(k) clearance on 2020-02-26. It is manufactured by 3D Systems. The 510(k) number is K192192.

When was VSP System approved by the FDA?

VSP System received FDA 510(k) clearance on 2020-02-26, under approval number K192192.

What company makes VSP System?

VSP System is manufactured by 3D Systems.

What is the FDA product code for VSP System?

The FDA product code for VSP System is DZJ.

Other Devices by 3D Systems

K193432Vantage PSI System K211244VSP® Orthopedics System K210347VSP System K214093VSP Bolus

Related Devices (Code: DZJ)

K181241KLS Martin Individual Patient Solutions (IPS) Planning SystemKLS-Martin L.P. K172164PROPEL DevicePropel Orthodontics, LLC K182789KLS Martin Individual Patient Solutions (IPS) Planning SystemKLS-Martin L.P. K193499DigiGuide SystemProtomed, Inc. K192282MedCAD® AccuPlan® SystemMedcad K181813ImmersiveView Surgical Plan (IVSP®)Immersivetouch

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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