Depuyacromed

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
48
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K040197EAGLE ANTERIOR CERVIAL PLATE SYSTEMApril 2, 2004
K031635DEPUY ACROMED VBR SYSTEMJune 23, 2003
K030833DEPUY ACROMED VBR SYSTEMApril 10, 2003
K030383MODIFICATION TO MOSS MIAMI SPINAL SYSTEM POLYAXIAL SCREWSFebruary 26, 2003
K030249SURGICAL TITANIUM MESH SYSTEMFebruary 14, 2003
K030103SUMMIT OCT SPINAL SYSTEM MINIPOLYAXIAL SCREWSFebruary 5, 2003
K023835DEVEX MESH SYSTEMJanuary 29, 2003
K024348MONARCH SPINE SYSTEMJanuary 28, 2003
K023804MOSS MIAMI SPINAL SYSTEM PIN NUTJanuary 23, 2003
K021039BOWTI ANTERIOR BUTTRESS STAPLE SYSTEMDecember 11, 2002
K023438MODIFICATION TO MONARCH SPINE SYSTEMNovember 13, 2002
K0226235.0 MM DIAMETER POLYAXIAL SCREWS (MOSS MIAMI 6.35MM SYSTEM)August 27, 2002
K022285MODIFICATION TO ISOLA SPINAL SYSTEMAugust 13, 2002
K022246MODIFICATION TO SYMPHONY GRAFT DELIVERY SYSTEMAugust 2, 2002
K022190MODIFICATION TO SUMMIT OCCIPITO-CERVICO-THORACIC (OCT) SPINAL SYSTEMJuly 24, 2002
K021335MONARCH SPINE SYSTEMJuly 11, 2002
K021879CROSSOVER CROSS CONNECTOR (ISOLA SPINAL SYSTEM)June 26, 2002
K021880CROSSOVER CROSS CONNECTOR (MOSS MIAMI SPINE SYSTEM)June 26, 2002
K021148MONARCH SPINE SYSTEM COMMERCIALLY PURE TITANIUM SPINAL RODMay 8, 2002
K020522MODIFICATION TO SURGICAL TITANIUM MESH SYSTEMMarch 21, 2002