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FDA 510(k)

NGARDE SYSTEM

K-Number: K072685 · 2007-10-19

ApplicantN Spine, Inc.
Decision Date2007-10-19
Product CodeNQP
Advisory CommitteeOR
DecisionUnknown

Device Summary

NGARDE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is N Spine, Inc.. It received FDA 510(k) clearance on 2007-10-19 under 510(k) number K072685. The device is classified under product code NQP. It was reviewed by the OR advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the NGARDE SYSTEM?

NGARDE SYSTEM is a medical device that received FDA 510(k) clearance on 2007-10-19. The listed applicant is N Spine, Inc.. The 510(k) number is K072685.

When did NGARDE SYSTEM receive FDA 510(k) clearance?

NGARDE SYSTEM received FDA 510(k) clearance on 2007-10-19, under 510(k) number K072685.

Who is the listed applicant for NGARDE SYSTEM?

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

What is the FDA product code for NGARDE SYSTEM?

The FDA product code for NGARDE SYSTEM is NQP.

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 N Spine, 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.

K061774NFIX II PEDICLE SCREW SYSTEMK053623NFIX FUSION SYSTEM

Related Devices (Code: NQP)

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.

K203678CD HORIZON™ Spinal SystemMedtronic Sofamor Danek USA, Inc.K191066CD Horizon™ Astute™ Spinal SystemMedtronic Sofamor Danek USA, Inc.K182928CD Horizon™ Spinal SystemMedtronic Sofamor Danek USA, Inc.K101704ZIMMER DTO PIN PRESS INSTRUMENTZimmer Spine, Inc.K101083DSS STABILIZATION SYSTEMParadigm Spine, LLCK092234DYNESYS TOP-LOADING SPINAL SYSTEMZimmer Spine, Inc.

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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