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FDA 510(k)

COHORT(TM) ANTERIOR PLATE SYSTEM (APS)

K-Number: K950011 · 1995-11-06

ApplicantCohort Medical Products Group, Inc.
Decision Date1995-11-06
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

COHORT(TM) ANTERIOR PLATE SYSTEM (APS) is the device name listed in this FDA 510(k) record. The listed applicant is Cohort Medical Products Group, Inc.. It received FDA 510(k) clearance on 1995-11-06 under 510(k) number K950011. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the COHORT(TM) ANTERIOR PLATE SYSTEM (APS)?

COHORT(TM) ANTERIOR PLATE SYSTEM (APS) is a medical device that received FDA 510(k) clearance on 1995-11-06. The listed applicant is Cohort Medical Products Group, Inc.. The 510(k) number is K950011.

When did COHORT(TM) ANTERIOR PLATE SYSTEM (APS) receive FDA 510(k) clearance?

COHORT(TM) ANTERIOR PLATE SYSTEM (APS) received FDA 510(k) clearance on 1995-11-06, under 510(k) number K950011.

Who is the listed applicant for COHORT(TM) ANTERIOR PLATE SYSTEM (APS)?

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

What is the FDA product code for COHORT(TM) ANTERIOR PLATE SYSTEM (APS)?

The FDA product code for COHORT(TM) ANTERIOR PLATE SYSTEM (APS) is KWQ.

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 Cohort Medical Products Group, 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.

K964975COHORT DISCECTOMY SYSTEMS (CDS)K943804BONE SCREWK943472COHORT AVB RETRACTOR SYSTEMK943474CANNULATED BONE SCREW

Related Devices (Code: KWQ)

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.

K262149corra® cervical plating systemCarlsmed, Inc.K261309Palisades™ Buttress Plate SystemBethesda Medical Devices, LLCK252776ARIES Anterior Cervical Plate SystemsZheJiang Decans Medical Devices Co., Ltd.K261112CastleLoc-P Anterior Cervical Plate SystemL&K BIOMED Co., Ltd.K260570corra™ cervical plating systemCarlsmed, Inc.K260697VyPlate™ Anterior Cervical Plate SystemVy Spine, LLC

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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