FDA 510(k)

미네랄 콜라겐 컴포지트 생물학적 모뎀블

K-번호: K182074 · 2019-03-21

결정일2019-03-21

제품 코드MQV

자문 위원회OR

결정Substantially Equivalent

기기 요약

Mineral Collagen Composite Bioactive Moldable 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 2019-03-21 under 510(k) number K182074. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Mineral Collagen Composite Bioactive Moldable?

Mineral Collagen Composite Bioactive Moldable is a medical device that received FDA 510(k) clearance on 2019-03-21. The listed applicant is Collagen Matrix, Inc.. The 510(k) number is K182074.

When did Mineral Collagen Composite Bioactive Moldable receive FDA 510(k) clearance?

Mineral Collagen Composite Bioactive Moldable received FDA 510(k) clearance on 2019-03-21, under 510(k) number K182074.

Who is the listed applicant for Mineral Collagen Composite Bioactive Moldable?

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 Mineral Collagen Composite Bioactive Moldable?

The FDA product code for Mineral Collagen Composite Bioactive Moldable is MQV.

Collagen Matrix, Inc.를 신청인으로 등재한 기타 기록

K251191콜라겐 드라 재생막 - 수리 K243071빠쿠스 피부 콜라겐 dermal 마トリックス K242302RejuvaKnee™ Collagen Meniscus Implant K233203Soft Tissue Augmentation Resorbable Matrix K240424미네랄 콜라겐 컴포지트 생물학적 조형성 뼈 기증 매트릭스 K231942미네랄 콜라겐 컴포지트 생활물질 추가 조형 가능

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