Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Ingenix Spinal System

K-Number: K241258 · 2024-06-04

Decision Date2024-06-04
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Ingenix Spinal System is a medical device manufactured by Ingenium Spine. It received FDA 510(k) clearance on 2024-06-04 under approval number K241258. 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 Ingenix Spinal System?

Ingenix Spinal System is a medical device that received FDA 510(k) clearance on 2024-06-04. It is manufactured by Ingenium Spine. The 510(k) number is K241258.

When was Ingenix Spinal System approved by the FDA?

Ingenix Spinal System received FDA 510(k) clearance on 2024-06-04, under approval number K241258.

What company makes Ingenix Spinal System?

Ingenix Spinal System is manufactured by Ingenium Spine.

What is the FDA product code for Ingenix Spinal System?

The FDA product code for Ingenix Spinal System is NKB.

Related Clinical Trials

Related PubMed Literature

Other Devices by Ingenium Spine

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.