FDA 510(k)

FG Bone Graft B

K-번호: K243745 · 2025-08-29

결정일2025-08-29

제품 코드LYC

자문 위원회DE

결정Substantially Equivalent

기기 요약

FG Bone Graft B is the device name listed in this FDA 510(k) record. The listed applicant is Full Golden Biotech Corporation. It received FDA 510(k) clearance on 2025-08-29 under 510(k) number K243745. The device is classified under product code LYC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the FG Bone Graft B?

FG Bone Graft B is a medical device that received FDA 510(k) clearance on 2025-08-29. The listed applicant is Full Golden Biotech Corporation. The 510(k) number is K243745.

When did FG Bone Graft B receive FDA 510(k) clearance?

FG Bone Graft B received FDA 510(k) clearance on 2025-08-29, under 510(k) number K243745.

Who is the listed applicant for FG Bone Graft B?

The FDA 510(k) record lists Full Golden Biotech Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FG Bone Graft B?

The FDA product code for FG Bone Graft B is LYC.

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FG Bone Graft B

기기 요약

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관련 임상시험

관련 기기 (코드: LYC)

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