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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
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
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127 records meeting your search criteria returned- Product Code: MAX Product Problem: Collapse Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
GLOBUS MEDICAL, INC. RISE 11/09/2017
SPINE WAVE, INC. LEVA TI PX DEVICE 07/20/2017
STRYKER ORTHOBIOLOGICS-MALVERN ACCULIF TL 8-12 MM X 11MM X 34 MM X 0 DE 06/26/2017
SPINE WAVE SPINE WAVE 06/08/2017
DEPUY SYNTHES SPINE STERILE OPTICAGE -G3 05/17/2017
DEPUY SYNTHES SPINE STERILE OPTICAGE -G3 05/17/2017
AMENDIA OMEGALIF 03/24/2017
STRYKER SPINE-US ACCULIF TL 8-12 MM X 11MM X 34 MM X 0 DE 02/24/2017
STRYKER SPINE-US ACCULIF TL 10-16 MM X 11 MM X 34 MM X 0 01/09/2017
STRYKER SPINE-US ACCULIF PL 8-12MM X 11MM X 27 MM X 8 DEG 01/06/2017
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