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)

XTEND-ST NUCLEUS REMOVAL SYSTEM, MODEL 9004

K-Number: K090303 · 2009-04-30

ApplicantCorespine Technologies, LLC
Decision Date2009-04-30
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

XTEND-ST NUCLEUS REMOVAL SYSTEM, MODEL 9004 is the device name listed in this FDA 510(k) record. The listed applicant is Corespine Technologies, LLC. It received FDA 510(k) clearance on 2009-04-30 under 510(k) number K090303. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the XTEND-ST NUCLEUS REMOVAL SYSTEM, MODEL 9004?

XTEND-ST NUCLEUS REMOVAL SYSTEM, MODEL 9004 is a medical device that received FDA 510(k) clearance on 2009-04-30. The listed applicant is Corespine Technologies, LLC. The 510(k) number is K090303.

When did XTEND-ST NUCLEUS REMOVAL SYSTEM, MODEL 9004 receive FDA 510(k) clearance?

XTEND-ST NUCLEUS REMOVAL SYSTEM, MODEL 9004 received FDA 510(k) clearance on 2009-04-30, under 510(k) number K090303.

Who is the listed applicant for XTEND-ST NUCLEUS REMOVAL SYSTEM, MODEL 9004?

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

What is the FDA product code for XTEND-ST NUCLEUS REMOVAL SYSTEM, MODEL 9004?

The FDA product code for XTEND-ST NUCLEUS REMOVAL SYSTEM, MODEL 9004 is HRX.

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

Related Devices (Code: HRX)

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.

K260203Fule Vertebroplasty Balloon CatheterBeijing Fule Science & Technology Development Co., Ltd.K254103HOPKINS Telescopes for ArthroscopyKarl Storz SE & CO. KGK252790Digital ClarusScope System and Digital NeuroPEN SystemClarus Medical, LLCK253523Freedom DS™ Decompression SystemSpinal SimplicityK252546VantageTM Lumbar Decompression KitAllevion Medical, LLCK253217MiiS Horus Arthroscope (EJA 100); MiiS Horus Endoscope Display System -Tablet (EDS 500); MiiS Horus Endoscope Display System -Video Box (EVS 700)Medimaging Integrated Solution, Inc (Miis)

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.

↑