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FDA 510(k)

CERVICORE CORPECTOMY CAGE

K-Number: K091426 · 2009-12-23

ApplicantVerticor, Ltd.
Decision Date2009-12-23
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CERVICORE CORPECTOMY CAGE is the device name listed in this FDA 510(k) record. The listed applicant is Verticor, Ltd.. It received FDA 510(k) clearance on 2009-12-23 under 510(k) number K091426. 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 CERVICORE CORPECTOMY CAGE?

CERVICORE CORPECTOMY CAGE is a medical device that received FDA 510(k) clearance on 2009-12-23. The listed applicant is Verticor, Ltd.. The 510(k) number is K091426.

When did CERVICORE CORPECTOMY CAGE receive FDA 510(k) clearance?

CERVICORE CORPECTOMY CAGE received FDA 510(k) clearance on 2009-12-23, under 510(k) number K091426.

Who is the listed applicant for CERVICORE CORPECTOMY CAGE?

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

What is the FDA product code for CERVICORE CORPECTOMY CAGE?

The FDA product code for CERVICORE CORPECTOMY CAGE 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 Verticor, Ltd. 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.

K110047VERTICOR K-WIRE SYSTEMK103137VENUS ANTERIOR CERVICAL PLATE

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.

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