Porous Biologic Scaffold
K-Number: K240765 · 2024-12-18
Device Summary
Frequently Asked Questions
What is the Porous Biologic Scaffold?
Porous Biologic Scaffold is a medical device that received FDA 510(k) clearance on 2024-12-18. The listed applicant is Ventris Medical. The 510(k) number is K240765.
When did Porous Biologic Scaffold receive FDA 510(k) clearance?
Porous Biologic Scaffold received FDA 510(k) clearance on 2024-12-18, under 510(k) number K240765.
Who is the listed applicant for Porous Biologic Scaffold?
The FDA 510(k) record lists Ventris Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Porous Biologic Scaffold?
The FDA product code for Porous Biologic Scaffold is MQV.
Other records listing Ventris Medical as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: MQV)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.