GREENS BRAND Posterior, Non-cervical Pedicle Screw Spinal System
K-Number: K230325 · 2024-10-10
Device Summary
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
Related PubMed Literature
Other Devices by Greens Surgicals Pvt. , Ltd.
Related Devices (Code: NKB)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.