FDA 510(k)

Vector Pedicle Screw System

K-Number: K241276 · 2024-05-20

Decision Date2024-05-20

Product CodeNKB

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

Vector Pedicle Screw System is a medical device manufactured by Innovasis, Inc.. It received FDA 510(k) clearance on 2024-05-20 under approval number K241276. 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 Vector Pedicle Screw System?

Vector Pedicle Screw System is a medical device that received FDA 510(k) clearance on 2024-05-20. It is manufactured by Innovasis, Inc.. The 510(k) number is K241276.

When was Vector Pedicle Screw System approved by the FDA?

Vector Pedicle Screw System received FDA 510(k) clearance on 2024-05-20, under approval number K241276.

What company makes Vector Pedicle Screw System?

Vector Pedicle Screw System is manufactured by Innovasis, Inc..

What is the FDA product code for Vector Pedicle Screw System?

The FDA product code for Vector Pedicle Screw System is NKB.

Related Clinical Trials

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Related PubMed Literature

PMID: 41487949 Verification, validation, and uncertainty quantification of finite element analysis results for pedicle screw assemblies under ASTM F1717 flexion and extension testing. Frontiers in bioengineering and biotechnology (2025)

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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.