FDA 510(k)

Gaudi Proximal Humerus Plate

K-번호: K241296 · 2024-07-23

결정일2024-07-23

제품 코드HRS

자문 위원회OR

결정Substantially Equivalent

기기 요약

Gaudi Proximal Humerus Plate is the device name listed in this FDA 510(k) record. The listed applicant is Netbiologics, LLC. It received FDA 510(k) clearance on 2024-07-23 under 510(k) number K241296. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Gaudi Proximal Humerus Plate?

Gaudi Proximal Humerus Plate is a medical device that received FDA 510(k) clearance on 2024-07-23. The listed applicant is Netbiologics, LLC. The 510(k) number is K241296.

When did Gaudi Proximal Humerus Plate receive FDA 510(k) clearance?

Gaudi Proximal Humerus Plate received FDA 510(k) clearance on 2024-07-23, under 510(k) number K241296.

Who is the listed applicant for Gaudi Proximal Humerus Plate?

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

What is the FDA product code for Gaudi Proximal Humerus Plate?

The FDA product code for Gaudi Proximal Humerus Plate is HRS.

공식 출처

FDA 데이터베이스에서 보기 →

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

Gaudi Proximal Humerus Plate

기기 요약

자주 묻는 질문

관련 임상시험

관련 기기 (코드: HRS)

공식 출처