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FDA 510(k)

GREENS BRAND Posterior, Non-cervical Pedicle Screw Spinal System

K-Number: K230325 · 2024-10-10

Decision Date2024-10-10
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

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

Frequently Asked Questions

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. It is manufactured by Greens Surgicals Pvt. , Ltd.. The 510(k) number is K230325.

When was GREENS BRAND Posterior, Non-cervical Pedicle Screw Spinal System approved by the FDA?

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

What company makes GREENS BRAND Posterior, Non-cervical Pedicle Screw Spinal System?

GREENS BRAND Posterior, Non-cervical Pedicle Screw Spinal System is manufactured by Greens Surgicals Pvt. , Ltd..

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.

Related Clinical Trials

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Official Source

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