VSP Orthopedics System
K-Number: K250711 · 2025-12-05
Applicant3D Systems, Inc.
Decision Date2025-12-05
Product CodePBF
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
VSP Orthopedics System is a medical device manufactured by 3D Systems, Inc.. It received FDA 510(k) clearance on 2025-12-05 under approval number K250711. The device is classified under product code PBF. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the VSP Orthopedics System?
VSP Orthopedics System is a medical device that received FDA 510(k) clearance on 2025-12-05. It is manufactured by 3D Systems, Inc.. The 510(k) number is K250711.
When was VSP Orthopedics System approved by the FDA?
VSP Orthopedics System received FDA 510(k) clearance on 2025-12-05, under approval number K250711.
What company makes VSP Orthopedics System?
VSP Orthopedics System is manufactured by 3D Systems, Inc..
What is the FDA product code for VSP Orthopedics System?
The FDA product code for VSP Orthopedics System is PBF.
Related Clinical Trials
Other Devices by 3D Systems, Inc.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.