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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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71 records meeting your search criteria returned- Product Code: HRS Product Problem: Device Inoperable Report Date From: 01/1/2016
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ManufacturerBrand NameDate Report Received
SMITH & NEPHEW, INC. 4.5MM PROX FEMUR LCK PLATE 9H R 234MM 11/07/2016
BIOMET MICROFIXATION STERNALOCK 360 MULTI-IMPLANT SYSTEM 10/24/2016
BIOMET MICROFIXATION 90 DEGREE CONTRA ANGLE SCREWDRIVER 10/21/2016
BIOMET MICROFIXATION BIOMET MICROFIXATION THORACIC FIXATION S 10/18/2016
BIOMET MICROFIXATION BIOMET MICROFIXATION THORACIC FIXATION S 10/18/2016
BIOMET MICROFIXATION 90 DEG CONTRA ANGLE SCREWDRIVER 10/14/2016
BIOMET MICROFIXATION 90 DEG CONTRA ANGLE SCREWDRIVER 10/13/2016
BIOMET MICROFIXATION STERNALOCK® 360 STERNAL CLOSURE SYSTEM 08/26/2016
BIOMET MICROFIXATION STERNALOCK 360 MULTI-IMPLANT SYSTEM 07/19/2016
STRYKER LEIBINGER FREIBURG CANNULATED COMPRESSION SCREW 06/21/2016
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