Mineral Collagen Composite Bioactive Moldable Bone Graft Matrix
K-Number: K240424 · 2024-03-12
Device Summary
Frequently Asked Questions
What is the Mineral Collagen Composite Bioactive Moldable Bone Graft Matrix?
Mineral Collagen Composite Bioactive Moldable Bone Graft Matrix is a medical device that received FDA 510(k) clearance on 2024-03-12. It is manufactured by Collagen Matrix, Inc.. The 510(k) number is K240424.
When was Mineral Collagen Composite Bioactive Moldable Bone Graft Matrix approved by the FDA?
Mineral Collagen Composite Bioactive Moldable Bone Graft Matrix received FDA 510(k) clearance on 2024-03-12, under approval number K240424.
What company makes Mineral Collagen Composite Bioactive Moldable Bone Graft Matrix?
Mineral Collagen Composite Bioactive Moldable Bone Graft Matrix is manufactured by Collagen Matrix, Inc..
What is the FDA product code for Mineral Collagen Composite Bioactive Moldable Bone Graft Matrix?
The FDA product code for Mineral Collagen Composite Bioactive Moldable Bone Graft Matrix is MQV.
Related Clinical Trials
Other Devices by Collagen Matrix, Inc.
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.