FDA 510(k)

개인 맞춤형 뇌면성형체 (CCI), 개인 맞춤형 뇌골체 (CSI)

K-번호: K182711 · 2019-05-21

결정일2019-05-21

제품 코드GWO

자문 위원회NE (이 문서는 원문이 제공되지 않았기 때문에 번역할 수 없습니다. 원문을 제공해 주시면 번역을 도와드리겠습니다.)

결정대체적으로 동일

기기 요약

Customized Craniofacial Implant (CCI), Customized Skull Implant (CSI) is the device name listed in this FDA 510(k) record. The listed applicant is Kelyniam Global, Inc.. It received FDA 510(k) clearance on 2019-05-21 under 510(k) number K182711. The device is classified under product code GWO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Customized Craniofacial Implant (CCI), Customized Skull Implant (CSI)?

Customized Craniofacial Implant (CCI), Customized Skull Implant (CSI) is a medical device that received FDA 510(k) clearance on 2019-05-21. The listed applicant is Kelyniam Global, Inc.. The 510(k) number is K182711.

When did Customized Craniofacial Implant (CCI), Customized Skull Implant (CSI) receive FDA 510(k) clearance?

Customized Craniofacial Implant (CCI), Customized Skull Implant (CSI) received FDA 510(k) clearance on 2019-05-21, under 510(k) number K182711.

Who is the listed applicant for Customized Craniofacial Implant (CCI), Customized Skull Implant (CSI)?

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

What is the FDA product code for Customized Craniofacial Implant (CCI), Customized Skull Implant (CSI)?

The FDA product code for Customized Craniofacial Implant (CCI), Customized Skull Implant (CSI) is GWO.

Kelyniam Global, Inc.를 신청인으로 등재한 기타 기록

K250334퓨전��면수술 임플란트; 퓨전 뼈 임플란트

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