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FDA 510(k)

STACKABLE CAGE SYSTEM

K-Number: K990148 · 1999-09-03

ApplicantDepuy Motech Acromed
Decision Date1999-09-03
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

STACKABLE CAGE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Depuy Motech Acromed. It received FDA 510(k) clearance on 1999-09-03 under 510(k) number K990148. 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 STACKABLE CAGE SYSTEM?

STACKABLE CAGE SYSTEM is a medical device that received FDA 510(k) clearance on 1999-09-03. The listed applicant is Depuy Motech Acromed. The 510(k) number is K990148.

When did STACKABLE CAGE SYSTEM receive FDA 510(k) clearance?

STACKABLE CAGE SYSTEM received FDA 510(k) clearance on 1999-09-03, under 510(k) number K990148.

Who is the listed applicant for STACKABLE CAGE SYSTEM?

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

What is the FDA product code for STACKABLE CAGE SYSTEM?

The FDA product code for STACKABLE CAGE 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 Depuy Motech Acromed 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.

K984350VSP SYSTEMK984348TIMX LOW BACK SYSTEMK982443DOC VENTRAL CERVICAL STABILIZATION SYSTEM

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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