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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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17 records meeting your search criteria returned- Product Code: NQO Patient Problem: Complaint, Ill-Defined Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
VERTIFLEX INC. SUPERION INDIRECT DECOMPRESSION SYSTEM 01/15/2021
BOSTON SCIENTIFIC NEUROMODULATION VERTIFLEX INSTRUMENT PLATFORM 01/11/2021
VERTIFLEX INC. SUPERION IDS KIT 09/10/2020
VERTIFLEX INC. SUPERION INDIRECT DECOMPRESSION SYSTEM 08/25/2020
VERTIFLEX INC. SUPERION INTERSPINOUS SPACER 08/19/2020
VERTIFLEX INC. VERTIFLEX INSTRUMENT PLATFORM 08/12/2020
VERTIFLEX INC. VERTIFLEX INSTRUMENT PLATFORM 08/12/2020
VERTIFLEX INC. SUPERION INDIRECT DECOMPRESSION SYSTEM 08/05/2020
VERTIFLEX INC. SUPERION IDS KIT 07/28/2020
VERTIFLEX INC. SUPERION INDIRECT DECOMPRESSION SYSTEM 07/14/2020
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