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FDA 510(k)

Anorganic Bone Mineral in Delivery Applicator

K-Number: K170541 · 2017-07-07

Decision Date2017-07-07
Product CodeNPM
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Anorganic Bone Mineral in Delivery Applicator is a medical device manufactured by Collagen Matrix, Inc.. It received FDA 510(k) clearance on 2017-07-07 under approval number K170541. The device is classified under product code NPM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.