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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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406 records meeting your search criteria returned- Product Code: MQP Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
K2M, INC. UNKNOWN_K2M_PRODUCT 12/07/2020
K2M, INC. UNKNOWN_K2M_PRODUCT 12/07/2020
K2M, INC. UNKNOWN_K2M_PRODUCT 12/07/2020
MEDTRONIC SOFAMOR DANEK USA, INC CAPSTONE L SPINAL SYSTEM 11/30/2020
MEDOS INTERNATIONAL SàRL CH UNKNOWN DEVEX CAGE/SPACER 11/10/2020
WRIGHTS LANE SYNTHES USA PRODUCTS LLC UNK - CAGE/SPACERS: ALIF 11/09/2020
MEDOS INTERNATIONAL SàRL CH UNKNOWN CAGE/SPACER 11/09/2020
WRIGHTS LANE SYNTHES USA PRODUCTS LLC UNK - CAGE/SPACERS: SYNCAGE 11/09/2020
OBERDORF SYNTHES PRODUKTIONS GMBH UNK - CAGE/SPACERS: SYNCAGE 11/09/2020
OBERDORF SYNTHES PRODUKTIONS GMBH UNK - CAGE/SPACERS: SYNCAGE 11/06/2020
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