VSP® Orthopedics System
K-Number: K211244 · 2021-11-10
Applicant3D Systems
Decision Date2021-11-10
Product CodePBF
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
VSP® Orthopedics System is a medical device manufactured by 3D Systems. It received FDA 510(k) clearance on 2021-11-10 under approval number K211244. 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 2021-11-10. It is manufactured by 3D Systems. The 510(k) number is K211244.
When was VSP® Orthopedics System approved by the FDA?
VSP® Orthopedics System received FDA 510(k) clearance on 2021-11-10, under approval number K211244.
What company makes VSP® Orthopedics System?
VSP® Orthopedics System is manufactured by 3D Systems.
What is the FDA product code for VSP® Orthopedics System?
The FDA product code for VSP® Orthopedics System is PBF.
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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.