DiversiVy Facet Screw System
K-Number: K253432 · 2026-03-19
Device Summary
DiversiVy Facet Screw System is a medical device manufactured by Vy Spine, LLC. It received FDA 510(k) clearance on 2026-03-19 under approval number K253432. The device is classified under product code MRW. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the DiversiVy Facet Screw System?
DiversiVy Facet Screw System is a medical device that received FDA 510(k) clearance on 2026-03-19. It is manufactured by Vy Spine, LLC. The 510(k) number is K253432.
When was DiversiVy Facet Screw System approved by the FDA?
DiversiVy Facet Screw System received FDA 510(k) clearance on 2026-03-19, under approval number K253432.
What company makes DiversiVy Facet Screw System?
DiversiVy Facet Screw System is manufactured by Vy Spine, LLC.
What is the FDA product code for DiversiVy Facet Screw System?
The FDA product code for DiversiVy Facet Screw System is MRW.
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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.