FDA 510(k)

배달 애플리케이터에 있는 결합 단백질과 비생성적인 뼈 무기질

K-번호: K171008 · 2017-10-30

결정일2017-10-30

제품 코드NPM

자문 위원회DE

결정Substantially Equivalent

기기 요약

Anorganic Bone Mineral with Collagen in Delivery Applicator is the device name listed in this FDA 510(k) record. The listed applicant is Collagen Matrix, Inc.. It received FDA 510(k) clearance on 2017-10-30 under 510(k) number K171008. The device is classified under product code NPM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Anorganic Bone Mineral with Collagen in Delivery Applicator?

Anorganic Bone Mineral with Collagen in Delivery Applicator is a medical device that received FDA 510(k) clearance on 2017-10-30. The listed applicant is Collagen Matrix, Inc.. The 510(k) number is K171008.

When did Anorganic Bone Mineral with Collagen in Delivery Applicator receive FDA 510(k) clearance?

Anorganic Bone Mineral with Collagen in Delivery Applicator received FDA 510(k) clearance on 2017-10-30, under 510(k) number K171008.

Who is the listed applicant for Anorganic Bone Mineral with Collagen in Delivery Applicator?

The FDA 510(k) record lists Collagen Matrix, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Anorganic Bone Mineral with Collagen in Delivery Applicator?

The FDA product code for Anorganic Bone Mineral with Collagen in Delivery Applicator is NPM.

Collagen Matrix, Inc.를 신청인으로 등재한 기타 기록

K251191Collagen Dura Regeneration Membrane - Repair K243071Bovine Dermis Collagen Dermal Matrix K242302RejuvaKnee™ Collagen Meniscus Implant K233203Soft Tissue Augmentation Resorbable Matrix K240424Mineral Collagen Composite Bioactive Moldable Bone Graft Matrix K231942Mineral Collagen Composite Bioactive Extra Moldable

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