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)

VERZA™ High Speed Drills

K-Number: K233638 · 2024-02-09

Decision Date2024-02-09
Product CodeOLO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

VERZA™ High Speed Drills is a medical device manufactured by Globus Medical, Inc.. It received FDA 510(k) clearance on 2024-02-09 under approval number K233638. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERZA™ High Speed Drills?

VERZA™ High Speed Drills is a medical device that received FDA 510(k) clearance on 2024-02-09. It is manufactured by Globus Medical, Inc.. The 510(k) number is K233638.

When was VERZA™ High Speed Drills approved by the FDA?

VERZA™ High Speed Drills received FDA 510(k) clearance on 2024-02-09, under approval number K233638.

What company makes VERZA™ High Speed Drills?

VERZA™ High Speed Drills is manufactured by Globus Medical, Inc..

What is the FDA product code for VERZA™ High Speed Drills?

The FDA product code for VERZA™ High Speed Drills is OLO.

Other Devices by Globus Medical, Inc.

View all 91 devices →

Related Devices (Code: OLO)

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.