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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
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113 records meeting your search criteria returned- Product Code: HSX Report Date From: 1/1/2017 Report Date To: 12/31/2017

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ManufacturerBrand NameDate Report Received
CONFORMIS, INC. IUNI G2 11/08/2017
CONFORMIS, INC. IUNI G2 11/08/2017
ZIMMER BIOMET, INC. PERSONA ANATOMIC TIBIAL SIZER MEDIAL 11/06/2017
MAKO SURGICAL CORP. UNKNOWN RESTORIS SZ 4 RIGHT MEDIAL TIBIA 10/31/2017
MAKO SURGICAL CORP. UNKNOWN RESTORIS SZ 3 RIGHT MEDIAL FEMOR 10/31/2017
ZIMMER BIOMET, INC. ARTICULAR SURFACE SIZE 4 10/23/2017
ZIMMER BIOMET, INC. ARTICULAR SURFACE SIZE 4 10/23/2017
ZIMMER BIOMET, INC. ZIMMER UNICOMPARTMENTAL KNEE SYSTEM TIBI 10/20/2017
ZIMMER BIOMET, INC. ZIMMER UNICOMPARTMENTAL KNEE SYSTEM ARTI 10/20/2017
ZIMMER BIOMET, INC. ZIMMER UNICOMPARTMENTAL KNEE SYSTEM FEMO 10/20/2017
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