FDA 510(k)

Triathlon® Total Knee System - Triathlon® Gold Femoral Components

K-번호: K252044 · 2025-10-24

신청자Howmedica Osteonics Corp., Dba Stryker Orthopaedics

결정일2025-10-24

제품 코드MBH

자문 위원회의료장비 규제 텍스트 번역 [회사명]의 [제품명]은 미국 식품의약국(FDA)에 등록된 의료장비로, 510(k) 신청을 통해 승인받았습니다. PMA(Premarket Approval) 신청이 진행 중이며, 연구 등록 번호(NCT)는 [NCT 번호]입니다. 논문 등록 번호(PMID)는 [PMID 번호]입니다. 더 자세한 정보는 다음 URL을 참조하세요: [URL] 정책: medical-regulatory-v1

결정대체적으로 동일

기기 요약

Triathlon® Total Knee System - Triathlon® Gold Femoral Components is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Osteonics Corp., Dba Stryker Orthopaedics. It received FDA 510(k) clearance on 2025-10-24 under 510(k) number K252044. The device is classified under product code MBH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Triathlon® Total Knee System - Triathlon® Gold Femoral Components?

Triathlon® Total Knee System - Triathlon® Gold Femoral Components is a medical device that received FDA 510(k) clearance on 2025-10-24. The listed applicant is Howmedica Osteonics Corp., Dba Stryker Orthopaedics. The 510(k) number is K252044.

When did Triathlon® Total Knee System - Triathlon® Gold Femoral Components receive FDA 510(k) clearance?

Triathlon® Total Knee System - Triathlon® Gold Femoral Components received FDA 510(k) clearance on 2025-10-24, under 510(k) number K252044.

Who is the listed applicant for Triathlon® Total Knee System - Triathlon® Gold Femoral Components?

The FDA 510(k) record lists Howmedica Osteonics Corp., Dba Stryker Orthopaedics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Triathlon® Total Knee System - Triathlon® Gold Femoral Components?

The FDA product code for Triathlon® Total Knee System - Triathlon® Gold Femoral Components is MBH.

Howmedica Osteonics Corp., Dba Stryker Orthopaedics를 신청인으로 등재한 기타 기록

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