Anorganic Bone Mineral in Delivery Applicator
K-Number: K170541 · 2017-07-07
Device Summary
Frequently Asked Questions
What is the Anorganic Bone Mineral in Delivery Applicator?
Anorganic Bone Mineral in Delivery Applicator is a medical device that received FDA 510(k) clearance on 2017-07-07. It is manufactured by Collagen Matrix, Inc.. The 510(k) number is K170541.
When was Anorganic Bone Mineral in Delivery Applicator approved by the FDA?
Anorganic Bone Mineral in Delivery Applicator received FDA 510(k) clearance on 2017-07-07, under approval number K170541.
What company makes Anorganic Bone Mineral in Delivery Applicator?
Anorganic Bone Mineral in Delivery Applicator is manufactured by Collagen Matrix, Inc..
What is the FDA product code for Anorganic Bone Mineral in Delivery Applicator?
The FDA product code for Anorganic Bone Mineral in Delivery Applicator is NPM.
Other Devices by Collagen Matrix, Inc.
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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.