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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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5 records meeting your search criteria returned- Product Code: HTY Product Problem: Material Frayed Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
ARTHREX, INC. BTB TIGHTROPE 01/12/2024
ARTHREX, INC. ACL TIGHTROPE WITH FIBERTAG 01/04/2024
ARTHREX, INC. ACL TIGHTROPE WITH FIBERTAG 07/21/2023
ARTHREX, INC. ACL TIGHTROPE RT 12/17/2014
ARTHREX, INC. ACL TIGHTROPE RT 10/29/2014
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