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FDA 510(k)

CREASPINE SUPSTANCE VERTEBRAL BODY REPLACEMENT SYSTEM

K-Number: K072537 · 2007-12-18

ApplicantCreaspine Sas
Decision Date2007-12-18
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CREASPINE SUPSTANCE VERTEBRAL BODY REPLACEMENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Creaspine Sas. It received FDA 510(k) clearance on 2007-12-18 under 510(k) number K072537. 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 CREASPINE SUPSTANCE VERTEBRAL BODY REPLACEMENT SYSTEM?

CREASPINE SUPSTANCE VERTEBRAL BODY REPLACEMENT SYSTEM is a medical device that received FDA 510(k) clearance on 2007-12-18. The listed applicant is Creaspine Sas. The 510(k) number is K072537.

When did CREASPINE SUPSTANCE VERTEBRAL BODY REPLACEMENT SYSTEM receive FDA 510(k) clearance?

CREASPINE SUPSTANCE VERTEBRAL BODY REPLACEMENT SYSTEM received FDA 510(k) clearance on 2007-12-18, under 510(k) number K072537.

Who is the listed applicant for CREASPINE SUPSTANCE VERTEBRAL BODY REPLACEMENT SYSTEM?

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

What is the FDA product code for CREASPINE SUPSTANCE VERTEBRAL BODY REPLACEMENT SYSTEM?

The FDA product code for CREASPINE SUPSTANCE VERTEBRAL BODY REPLACEMENT SYSTEM is MQP.

Related Clinical Trials

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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