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)

MODIFICATION TO VERTEBRON SCP CERVICAL PLATE SYSTEM

K-Number: K043181 · 2004-12-17

ApplicantVertebron, Inc.
Decision Date2004-12-17
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO VERTEBRON SCP CERVICAL PLATE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Vertebron, Inc.. It received FDA 510(k) clearance on 2004-12-17 under 510(k) number K043181. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION TO VERTEBRON SCP CERVICAL PLATE SYSTEM?

MODIFICATION TO VERTEBRON SCP CERVICAL PLATE SYSTEM is a medical device that received FDA 510(k) clearance on 2004-12-17. The listed applicant is Vertebron, Inc.. The 510(k) number is K043181.

When did MODIFICATION TO VERTEBRON SCP CERVICAL PLATE SYSTEM receive FDA 510(k) clearance?

MODIFICATION TO VERTEBRON SCP CERVICAL PLATE SYSTEM received FDA 510(k) clearance on 2004-12-17, under 510(k) number K043181.

Who is the listed applicant for MODIFICATION TO VERTEBRON SCP CERVICAL PLATE SYSTEM?

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

What is the FDA product code for MODIFICATION TO VERTEBRON SCP CERVICAL PLATE SYSTEM?

The FDA product code for MODIFICATION TO VERTEBRON SCP CERVICAL PLATE SYSTEM is KWQ.

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 Vertebron, Inc. 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.

K081567VERTEBRON SSP CERVICAL PLATING SYSTEMK081597MODIFICATION TO VERTEBRON PSS PEDICLE SCREW SYSTEMK073502VERTEBRON VBR SYSTEMK071376MODIFICATION TO VERTEBRON PSS PEDICLE SCREW SYSTEMK062110VERTEBRON SCP CERVICAL PLATE SYSTEMK051815MODIFICATION TO VERTEBRON SCP CERVICAL PLATE SYSTEM

View all 11 devices →

Related Devices (Code: KWQ)

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.

K262149corra® cervical plating systemCarlsmed, Inc.K261309Palisades™ Buttress Plate SystemBethesda Medical Devices, LLCK252776ARIES Anterior Cervical Plate SystemsZheJiang Decans Medical Devices Co., Ltd.K261112CastleLoc-P Anterior Cervical Plate SystemL&K BIOMED Co., Ltd.K260570corra™ cervical plating systemCarlsmed, Inc.K260697VyPlate™ Anterior Cervical Plate SystemVy Spine, LLC

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.

↑