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)

NUVASIVE COROENT EXTENSURE SYSTEM

K-Number: K052210 · 2005-12-12

ApplicantNuvasive, Inc.
Decision Date2005-12-12
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NUVASIVE COROENT EXTENSURE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Nuvasive, Inc.. It received FDA 510(k) clearance on 2005-12-12 under 510(k) number K052210. 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 NUVASIVE COROENT EXTENSURE SYSTEM?

NUVASIVE COROENT EXTENSURE SYSTEM is a medical device that received FDA 510(k) clearance on 2005-12-12. The listed applicant is Nuvasive, Inc.. The 510(k) number is K052210.

When did NUVASIVE COROENT EXTENSURE SYSTEM receive FDA 510(k) clearance?

NUVASIVE COROENT EXTENSURE SYSTEM received FDA 510(k) clearance on 2005-12-12, under 510(k) number K052210.

Who is the listed applicant for NUVASIVE COROENT EXTENSURE SYSTEM?

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

What is the FDA product code for NUVASIVE COROENT EXTENSURE SYSTEM?

The FDA product code for NUVASIVE COROENT EXTENSURE 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 Nuvasive, 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.

K240507NuVasive AttraX ScaffoldK223731NuVasive Modulus-C Interbody SystemK211757Simplify DiscK173117NuVasive® VersaTie™ SystemK133052AFFIX(R) NEXT GEN SPINOUS PROCESS PLATE SYSTEMK131025ARCHON ANTERIOR CERVICAL PLATE SYSTEM

View all 85 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.

↑