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U.S. Department of Health and Human Services

510(k) Premarket Notification
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1 to 10 of 11 Results
ProductCode: FTL Applicant: ATRIUM MEDICAL CORP. Decision Date To: 04/26/2024
 
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510(K)
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c-qur rpm mesh ATRIUM MEDICAL CORP. K121070 04/26/2012
atrium c-qur ovt mesh ATRIUM MEDICAL CORP. K100076 01/26/2010
c-qur v -patch mesh ATRIUM MEDICAL CORP. K090909 06/04/2009
atrium prolite s mesh ATRIUM MEDICAL CORP. K082748 01/14/2009
c-qur edge mesh v-patch ATRIUM MEDICAL CORP. K080691 04/16/2008
c-qur lite mesh v-patch ATRIUM MEDICAL CORP. K080688 04/16/2008
atrium prolite ultra s mesh ATRIUM MEDICAL CORP. K070192 03/08/2007
atrium medical corporation c-qur mesh ATRIUM MEDICAL CORP. K050311 03/31/2006
atrium lite mesh ATRIUM MEDICAL CORP. K002093 07/24/2000
atrium medical corporation advanta ptfe facial implant ATRIUM MEDICAL CORP. K992991 01/27/2000
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