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)

HUMERUS WIRES

K-Number: K964243 · 1996-12-05

ApplicantCompagnie Financiere & Medicale (Cf&M)
Decision Date1996-12-05
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

HUMERUS WIRES is the device name listed in this FDA 510(k) record. The listed applicant is Compagnie Financiere & Medicale (Cf&M). It received FDA 510(k) clearance on 1996-12-05 under 510(k) number K964243. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HUMERUS WIRES?

HUMERUS WIRES is a medical device that received FDA 510(k) clearance on 1996-12-05. The listed applicant is Compagnie Financiere & Medicale (Cf&M). The 510(k) number is K964243.

When did HUMERUS WIRES receive FDA 510(k) clearance?

HUMERUS WIRES received FDA 510(k) clearance on 1996-12-05, under 510(k) number K964243.

Who is the listed applicant for HUMERUS WIRES?

The FDA 510(k) record lists Compagnie Financiere & Medicale (Cf&M) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HUMERUS WIRES?

The FDA product code for HUMERUS WIRES is HSB.

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: HSB)

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.

K261345Pediatric Nailing Platform FemurOrthoPediatrics Corp.K261481Pangea Femur Reconstruction SystemStryker GmbHK253080AND Medical Femoral Nail System (PFNA01); AND Medical Femoral Nail System (PFNA02)Suzhou and Science & Technology Development Corp.K261651Precice™ Max System and Precice™ Ankle Salvage SystemNuVasive Specialized OrthopedicsK253155Fule Metallic Lockable Intramedullary Nail SystemsBeijing Fule Science & Technology Development Co., Ltd.K253046HERA Interlocking Intramedullary Nailing SystemZheJiang Decans Medical Devices Co., Ltd.

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.

↑