FDA 510(k)

Xenograft Bovine Bone Particulate

K-번호: K240133 · 2024-08-16

결정일2024-08-16

제품 코드NPM

자문 위원회DE

결정Substantially Equivalent

기기 요약

Xenograft Bovine Bone Particulate is the device name listed in this FDA 510(k) record. The listed applicant is Collagen Solutions, LLC. It received FDA 510(k) clearance on 2024-08-16 under 510(k) number K240133. 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 Xenograft Bovine Bone Particulate?

Xenograft Bovine Bone Particulate is a medical device that received FDA 510(k) clearance on 2024-08-16. The listed applicant is Collagen Solutions, LLC. The 510(k) number is K240133.

When did Xenograft Bovine Bone Particulate receive FDA 510(k) clearance?

Xenograft Bovine Bone Particulate received FDA 510(k) clearance on 2024-08-16, under 510(k) number K240133.

Who is the listed applicant for Xenograft Bovine Bone Particulate?

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

What is the FDA product code for Xenograft Bovine Bone Particulate?

The FDA product code for Xenograft Bovine Bone Particulate is NPM.

공식 출처

FDA 데이터베이스에서 보기 →

FDA Open API에서 수집된 데이터입니다. 가장 정확하고 공인된 정보는 항상 공식 레코드를 참조하시기 바랍니다.

Xenograft Bovine Bone Particulate

기기 요약

자주 묻는 질문

관련 임상시험

관련 기기 (코드: NPM)

공식 출처