Porous Biologic Scaffold
K-Number: K250556 · 2025-03-21
ApplicantVentris Medical
Decision Date2025-03-21
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Porous Biologic Scaffold is a medical device manufactured by Ventris Medical. It received FDA 510(k) clearance on 2025-03-21 under approval number K250556. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Porous Biologic Scaffold?
Porous Biologic Scaffold is a medical device that received FDA 510(k) clearance on 2025-03-21. It is manufactured by Ventris Medical. The 510(k) number is K250556.
When was Porous Biologic Scaffold approved by the FDA?
Porous Biologic Scaffold received FDA 510(k) clearance on 2025-03-21, under approval number K250556.
What company makes Porous Biologic Scaffold?
Porous Biologic Scaffold is manufactured by Ventris Medical.
What is the FDA product code for Porous Biologic Scaffold?
The FDA product code for Porous Biologic Scaffold is MQV.
Other Devices by Ventris Medical
Related Devices (Code: MQV)
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.