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)

PROTOE ENDOSORB SMALL HAMMER TOE PIN

K-Number: K100414 · 2010-07-02

ApplicantMerete Medical GmbH
Decision Date2010-07-02
Product CodeJDW
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PROTOE ENDOSORB SMALL HAMMER TOE PIN is the device name listed in this FDA 510(k) record. The listed applicant is Merete Medical GmbH. It received FDA 510(k) clearance on 2010-07-02 under 510(k) number K100414. The device is classified under product code JDW. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROTOE ENDOSORB SMALL HAMMER TOE PIN?

PROTOE ENDOSORB SMALL HAMMER TOE PIN is a medical device that received FDA 510(k) clearance on 2010-07-02. The listed applicant is Merete Medical GmbH. The 510(k) number is K100414.

When did PROTOE ENDOSORB SMALL HAMMER TOE PIN receive FDA 510(k) clearance?

PROTOE ENDOSORB SMALL HAMMER TOE PIN received FDA 510(k) clearance on 2010-07-02, under 510(k) number K100414.

Who is the listed applicant for PROTOE ENDOSORB SMALL HAMMER TOE PIN?

The FDA 510(k) record lists Merete Medical GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PROTOE ENDOSORB SMALL HAMMER TOE PIN?

The FDA product code for PROTOE ENDOSORB SMALL HAMMER TOE PIN is JDW.

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 Merete Medical GmbH 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.

K160548MC-Subtalar(TM) IIK152187MetaFix LS Locking Screws, Merete Cannulated PCS, Merete CS Cortical Screws, Merete Cannulated HCS, DuoThread Scarf Screws and TwistCut Snap-Off ScrewsK132226METAFIX BLP PLATE, SIZE 31, LEFT, METAFIX BLP PLATE, SIZE 31,RIGHTK123619INTRABLOCK BIOBALL HIP SYSTEM (IBS)K130400MERETEC CS, CORTICAL SCREWSK120787MERETE LOCKING BONE PLATE SYSTEM III

View all 20 devices →

Related Devices (Code: JDW)

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.

K260073XT3 System; XT3 System, Mini; XT3 System, 40mm; XT3 System, Mini, 40mmBiodynamik, Inc.K250316Meduloc Intramedullary Fracture Fixation (IFF) SystemMeduloc, LLCK241357XT3 SystemBiodynamik, Inc.K223112MAVERICK Mini External Fixation SystemSmith & Nephew, Inc.K213874MAVERICK External Fixation SystemSmith & Nephew, Inc.K211508Steinmann Pins and Kirschner WiresStryker GmbH

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.

↑