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

FDA 510(k)

DEPUY ACROMED VBR SYSTEM

K-Number: K030833 · 2003-04-10

ApplicantDepuyacromed
Decision Date2003-04-10
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DEPUY ACROMED VBR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Depuyacromed. It received FDA 510(k) clearance on 2003-04-10 under 510(k) number K030833. The device is classified under product code MQP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEPUY ACROMED VBR SYSTEM?

DEPUY ACROMED VBR SYSTEM is a medical device that received FDA 510(k) clearance on 2003-04-10. The listed applicant is Depuyacromed. The 510(k) number is K030833.

When did DEPUY ACROMED VBR SYSTEM receive FDA 510(k) clearance?

DEPUY ACROMED VBR SYSTEM received FDA 510(k) clearance on 2003-04-10, under 510(k) number K030833.

Who is the listed applicant for DEPUY ACROMED VBR SYSTEM?

The FDA 510(k) record lists Depuyacromed as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DEPUY ACROMED VBR SYSTEM?

The FDA product code for DEPUY ACROMED VBR SYSTEM is MQP.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Depuyacromed as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K040197EAGLE ANTERIOR CERVIAL PLATE SYSTEMK031635DEPUY ACROMED VBR SYSTEMK030383MODIFICATION TO MOSS MIAMI SPINAL SYSTEM POLYAXIAL SCREWSK030249SURGICAL TITANIUM MESH SYSTEMK030103SUMMIT OCT SPINAL SYSTEM MINIPOLYAXIAL SCREWSK023835DEVEX MESH SYSTEM

View all 48 devices →

Related Devices (Code: MQP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261810Vertiwedge® Intraosseous SystemFoundation Surgical GroupK261031POSEIDON STSignus Medinzintechnik GmbHK253158VyBrate™ VBR SystemVy Spine, LLCK241468Vertiwedge® Intraosseous SystemFoundation Surgical Group, Inc.K232790KONG®-TL VBR System and KONG® C VBR SystemIcotec AGK233359DOMINION Expandable Corpectomy SystemAstura Medical

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.

↑