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)

COHORT AVB RETRACTOR SYSTEM

K-Number: K943472 · 1994-10-20

ApplicantCohort Medical Products Group, Inc.
Decision Date1994-10-20
Product CodeHXB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

COHORT AVB RETRACTOR SYSTEM 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 1994-10-20 under 510(k) number K943472. The device is classified under product code HXB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COHORT AVB RETRACTOR SYSTEM?

COHORT AVB RETRACTOR SYSTEM is a medical device that received FDA 510(k) clearance on 1994-10-20. The listed applicant is Cohort Medical Products Group, Inc.. The 510(k) number is K943472.

When did COHORT AVB RETRACTOR SYSTEM receive FDA 510(k) clearance?

COHORT AVB RETRACTOR SYSTEM received FDA 510(k) clearance on 1994-10-20, under 510(k) number K943472.

Who is the listed applicant for COHORT AVB RETRACTOR SYSTEM?

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 AVB RETRACTOR SYSTEM?

The FDA product code for COHORT AVB RETRACTOR SYSTEM is HXB.

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)K950011COHORT(TM) ANTERIOR PLATE SYSTEM (APS)K943804BONE SCREWK943474CANNULATED BONE SCREW

Related Devices (Code: HXB)

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.

K960539DIAO HAND SURGERY SETKinetikos Medical, Inc.K912843FLEXMEDICS RETRACT ORTH PROBE, PETTINE BONE PROBEFlexmedicsK890227SURGICAL PROBEKinetic Medical ProductsK873652HOOK PROBE #TM-1376Arthropedics, Inc.K873651BLUNT MEASURING PROBE W/2MM GRADATIONS #TM-1375Arthropedics, Inc.K863149BOWEN PROBEBowen & Company, 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.

↑