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Specialty Surgical Products, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
13
Inspections
3
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K140383ALLOX2 TISSUE EXPANDERSOctober 28, 2014
K070303SILICONE TISSUE EXPANDERJune 22, 2007
K984106MAMMARY SIZER, MAMMARY PROTHESIS SIZERFebruary 12, 1999
K983015VIRILIS PENILE PROSTHESISFebruary 5, 1999
K982258MAMMARY SIZERSeptember 8, 1998
K982065STERILE SILICONE EXTERNAL WOUND COVERAugust 12, 1998
K982067MAGNETIC PORT SILICONE TISSUE EXPANDERJuly 13, 1998
K974653SILICONE ELASTOMER SHEETINGMarch 13, 1998
K974654SILICONE BLOCKSFebruary 24, 1998
K974209SILICONE TISSUE/INFLATABLE TISSUE EXPANDERFebruary 6, 1998
K973656DISPOSABLE SILICONE EPISTAXIS CATHETERNovember 18, 1997
K973082VENTRAL WALL DEFECT REDUCTION SILONovember 4, 1997
K973114SILICONE BILIARY STENT/BILIARY CATHETERSeptember 19, 1997