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FDA 510(k)

VERTEBRON VBR SYSTEM

K-Number: K073502 · 2008-03-24

ApplicantVertebron, Inc.
Decision Date2008-03-24
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VERTEBRON VBR 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 2008-03-24 under 510(k) number K073502. 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 VERTEBRON VBR SYSTEM?

VERTEBRON VBR SYSTEM is a medical device that received FDA 510(k) clearance on 2008-03-24. The listed applicant is Vertebron, Inc.. The 510(k) number is K073502.

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

VERTEBRON VBR SYSTEM received FDA 510(k) clearance on 2008-03-24, under 510(k) number K073502.

Who is the listed applicant for VERTEBRON VBR 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 VERTEBRON VBR SYSTEM?

The FDA product code for VERTEBRON VBR SYSTEM is MQP.

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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 SYSTEMK071376MODIFICATION TO VERTEBRON PSS PEDICLE SCREW SYSTEMK062110VERTEBRON SCP CERVICAL PLATE SYSTEMK051815MODIFICATION TO VERTEBRON SCP CERVICAL PLATE SYSTEMK051716VERTEBRON PSS PEDICLE SCREW SYSTEM

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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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