Stimulator, spinal-cord, totally implanted for pain relief
PMA 번호: P030017 · 2026-09-22
광고
기기 요약
Stimulator, spinal-cord, totally implanted for pain relief is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corp. It received FDA 510(k) clearance on 2026-09-22. The device is classified under product code LGW. It was reviewed by the NE advisory panel.
자주 묻는 질문
What is the Stimulator, spinal-cord, totally implanted for pain relief?
Stimulator, spinal-cord, totally implanted for pain relief is a medical device that received FDA 510(k) clearance on 2026-09-22. The listed applicant is Boston Scientific Corp.
When did Stimulator, spinal-cord, totally implanted for pain relief receive FDA 510(k) clearance?
The clearance date for Stimulator, spinal-cord, totally implanted for pain relief can be found in the official FDA records.
Who is the listed applicant for Stimulator, spinal-cord, totally implanted for pain relief?
The FDA 510(k) record lists Boston Scientific Corp as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Stimulator, spinal-cord, totally implanted for pain relief?
The FDA product code for Stimulator, spinal-cord, totally implanted for pain relief is LGW.
관련 임상시험
관련 기록은 이름, 제품 코드 또는 기타 메타데이터를 사용하여 자동으로 매칭됩니다. 매칭은 검증된 임상, 과학, 기업 또는 규제 상의 관계를 입증하지 않으며, 연결된 공식 출처를 검토하시기 바랍니다.
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공식 출처
FDA 데이터베이스에서 보기 →FDA Open API에서 수집된 데이터입니다. 가장 정확하고 공인된 정보는 항상 공식 레코드를 참조하시기 바랍니다.
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