FDA 510(k)

Lucent® XP

K-번호: K234150 · 2024-03-27

결정일2024-03-27

제품 코드MAX

자문 위원회OR

결정Substantially Equivalent

기기 요약

Lucent® XP is the device name listed in this FDA 510(k) record. The listed applicant is Spinal Elements. It received FDA 510(k) clearance on 2024-03-27 under 510(k) number K234150. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Lucent® XP?

Lucent® XP is a medical device that received FDA 510(k) clearance on 2024-03-27. The listed applicant is Spinal Elements. The 510(k) number is K234150.

When did Lucent® XP receive FDA 510(k) clearance?

Lucent® XP received FDA 510(k) clearance on 2024-03-27, under 510(k) number K234150.

Who is the listed applicant for Lucent® XP?

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

What is the FDA product code for Lucent® XP?

The FDA product code for Lucent® XP is MAX.

관련 기기 (코드: MAX)

공식 출처

FDA 데이터베이스에서 보기 →

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

기기 요약

자주 묻는 질문

관련 임상시험

관련 기기 (코드: MAX)

공식 출처