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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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82 records meeting your search criteria returned- Product Code: OUR Patient Problem: Joint Disorder Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
SI-BONE, INC. IFUSE IMPLANT SYSTEM 02/14/2018
SI-BONE, INC. IFUSE IMPLANT SYSTEM 05/26/2017
SI-BONE, INC. IFUSE IMPLANT SYSTEM 05/18/2017
SI-BONE, INC. IFUSE IMPLANT SYSTEM 05/05/2017
SI-BONE, INC. IFUSE IMPLANT SYSTEM 04/13/2017
SI-BONE, INC. IFUSE IMPLANT SYSTEM 04/04/2017
SI-BONE, INC. IFUSE IMPLANT SYSTEM 03/30/2017
SI-BONE, INC. IFUSE IMPLANT SYSTEM 03/28/2017
SI-BONE, INC. IFUSE IMPLANT SYSTEM 03/28/2017
SI-BONE, INC. IFUSE IMPLANT SYSTEM 03/24/2017
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