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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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7 records meeting your search criteria returned- Product Code: MBI Product Problem: Failure to Disconnect Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
ROTATION MEDICAL, INC. BONE ANCHORS 3 W ARTHRO DEL SYSTEM 07/30/2020
MEDOS INTERNATIONAL SàRL TRUESPAN 12 DEGREE PLGA 12/26/2019
MEDOS INTERNATIONAL SàRL TRUESPAN 12 DEGREE PLGA 12/24/2019
SMITH & NEPHEW, INC. FOOTPRINT ULTRA PK SUTURE ANCHOR, 5.5 05/02/2017
ARTHROCARE CORPORATION ARTHROCARE 09/29/2015
BIOMET ORTHOPEDICS MAXFIRE MARXMEN STRAIGHT 12/29/2014
ARTHROCARE CORP SPEEDSCREW 5.5 IMPLANT WITH INSERTER HAN 09/18/2014
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