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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
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192 records meeting your search criteria returned- Product Code: LXH Product Problem: Device Contamination with Chemical or Other Material Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
WRIGHT MEDICAL TECHNOLOGY, INC. VALOR(R) TTC FUSION INSTRUMENT SET 09/28/2016
STRYKER TRAUMA KIEL GUIDE WIRE, SMOOTH-TIPPED, STERILE T2 HU 08/11/2016
STRYKER TRAUMA KIEL TISSUE PROTECTION SLEEVE T2 RECON 07/19/2016
STRYKER TRAUMA KIEL TISSUE PROTECTION SLEEVE T2 RECON 07/19/2016
STRYKER TRAUMA KIEL UNKNOWN T2 RECON CANNULATED INSTRUMENTS 07/19/2016
STRYKER TRAUMA KIEL K-WIRE, STERILE T2 FEMUR Ø1,8X310 MM 06/10/2016
STRYKER TRAUMA KIEL GUIDE WIRE, BALL-TIPPED, STERILE T2 FEMU 06/03/2016
STRYKER TRAUMA KIEL K-WIRE, STERILE T2 FEMUR Ø3X285 MM 04/08/2016
STRYKER TRAUMA KIEL GUIDE WIRE, BALL-TIPPED, STERILE T2 FEMU 04/08/2016
STRYKER TRAUMA KIEL REAMER SHAFT, MOD.TRINKLE BIXCUT Ø8.0X44 04/07/2016
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