FDA 510(k)

GREENS BRAND Posterior, Non-cervical Pedicle Screw Spinal System

K-번호: K230325 · 2024-10-10

결정일2024-10-10

제품 코드NKB

자문 위원회OR

결정Substantially Equivalent

기기 요약

GREENS BRAND Posterior, Non-cervical Pedicle Screw Spinal System is the device name listed in this FDA 510(k) record. The listed applicant is Greens Surgicals Pvt. , Ltd.. It received FDA 510(k) clearance on 2024-10-10 under 510(k) number K230325. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the GREENS BRAND Posterior, Non-cervical Pedicle Screw Spinal System?

GREENS BRAND Posterior, Non-cervical Pedicle Screw Spinal System is a medical device that received FDA 510(k) clearance on 2024-10-10. The listed applicant is Greens Surgicals Pvt. , Ltd.. The 510(k) number is K230325.

When did GREENS BRAND Posterior, Non-cervical Pedicle Screw Spinal System receive FDA 510(k) clearance?

GREENS BRAND Posterior, Non-cervical Pedicle Screw Spinal System received FDA 510(k) clearance on 2024-10-10, under 510(k) number K230325.

Who is the listed applicant for GREENS BRAND Posterior, Non-cervical Pedicle Screw Spinal System?

The FDA 510(k) record lists Greens Surgicals Pvt. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GREENS BRAND Posterior, Non-cervical Pedicle Screw Spinal System?

The FDA product code for GREENS BRAND Posterior, Non-cervical Pedicle Screw Spinal System is NKB.

Greens Surgicals Pvt. , Ltd.를 신청인으로 등재한 기타 기록

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