ClearanceBrief
Company ยท US

Cormatrix Cardiovascular, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2005 to 2018. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DXZPatch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene5
FTMMesh, Surgical1
PSQIntracardiac Patch Or Pledget, Biologically Derived1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Oct 10, 2018K181038CorMatrix Cor Patch (3 cm x 5 cm)(single pack), CorMatrix Cor Patch (4 cm x 7 cm)(single pack), CorMatrix Cor Patch (7 c
Cormatrix Cardiovascular, Inc.
PSQ
Feb 4, 2016K152127CorMatrix Tyke
Cormatrix Cardiovascular, Inc.
DXZ
Aug 15, 2014K140306CORMATRIX PROTECT ECM ENVELOPE
Cormatrix Cardiovascular, Inc.
FTM
Jul 15, 2014K140789CORMATRIX ECM FOR VASCULAR REPAIR
Cormatrix Cardiovascular, Inc.
DXZ
Jul 26, 2011K111187PATCH, PLEDGET AND INTRACARDIAC
Cormatrix Cardiovascular, Inc.
DXZ
Feb 16, 2007K063349CORMATRIX PATCH FOR CARDIAC TISSUE REPAIR
Cormatrix Cardiovascular, Inc.
DXZ
Aug 31, 2005K051405REGENSIS PERICARDIAL PATCH
Cormatrix Cardiovascular, Inc.
DXZ

Latest recalls

DateFirm and productCodeLinked 510(k)
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