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)

TITANIUM TELEGRAPH HUMERAL NAIL

K-Number: K042332 · 2004-10-07

ApplicantFournitures Hospitalieres Industrie
Decision Date2004-10-07
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TITANIUM TELEGRAPH HUMERAL NAIL is the device name listed in this FDA 510(k) record. The listed applicant is Fournitures Hospitalieres Industrie. It received FDA 510(k) clearance on 2004-10-07 under 510(k) number K042332. 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 TITANIUM TELEGRAPH HUMERAL NAIL?

TITANIUM TELEGRAPH HUMERAL NAIL is a medical device that received FDA 510(k) clearance on 2004-10-07. The listed applicant is Fournitures Hospitalieres Industrie. The 510(k) number is K042332.

When did TITANIUM TELEGRAPH HUMERAL NAIL receive FDA 510(k) clearance?

TITANIUM TELEGRAPH HUMERAL NAIL received FDA 510(k) clearance on 2004-10-07, under 510(k) number K042332.

Who is the listed applicant for TITANIUM TELEGRAPH HUMERAL NAIL?

The FDA 510(k) record lists Fournitures Hospitalieres Industrie as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TITANIUM TELEGRAPH HUMERAL NAIL?

The FDA product code for TITANIUM TELEGRAPH HUMERAL NAIL 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

Other records listing Fournitures Hospitalieres Industrie 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.

K171789ARROW Reverse Porous GlenoidK163148BePOD® Foot ScrewsK163710BePOD® EZ Weil ScrewsK162068ARROW Anatomical Porous glenoidK170040BePOD Cannulated Arthrodesis ScrewsK120740COLS® FIXATION SYSTEM

View all 20 devices →

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.

↑