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Macropore Biosurgery, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
17
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K042261MACROPORE PURICEL LIPOPLASTY SYSTEMSeptember 20, 2004
K041105MACROPORE HYDROSORB SPINE SYSTEMJuly 28, 2004
K031955MACROPORE SURGI-WRAP MAST BIORESORBABLE SHEETSeptember 22, 2003
K031785MACROPORE CARDIO-WRAP (TS)September 4, 2003
K024169MACROPORE OS RECONSTRUCTIONJuly 1, 2003
K023643MACROPORE SURGICAL BARRIER FILMFebruary 21, 2003
K021164MACROPORE OS TRAUMAJuly 1, 2002
K012025MACROPORE SURGIWRAP (TS)December 3, 2001
K012769MACROPORE ENT RECONSTRUCTION FILMOctober 25, 2001
K012413MACROPORE FX, PS, NS, LPSeptember 18, 2001
K011715MACROPORE IB RESORBABLE PLUGAugust 27, 2001
K010911MACROPORE OS SPINAL SYSTEMJuly 20, 2001
K002207MACROPOREPX PEDIATRIC SYSTEMJuly 11, 2001
K002334MACROPORENS CRANILOCMay 2, 2001
K000696MACROPOREMX MANDIBULAR FIXATION SYSTEMOctober 19, 2000
K994158MACROSORBOS PROTECTIVE SHEETJuly 24, 2000
K000992MACROPOREDX DISTRACTOR SYSTEMJune 26, 2000