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Kinetikos Medical, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
19
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K061749ECLIPSE TOTAL ANKLE IMPLANTNovember 22, 2006
K061465KMI CEMENT RESTRICTOR IMPLANTOctober 5, 2006
K051611MBARESORB IMPLANTSeptember 6, 2005
K041461KMI DISTAL VOLAR RADIUS PLATE SYSTEMAugust 16, 2004
K032806KATALYST RADIAL HEAD IMPLANTApril 16, 2004
K040356KOMPRESSOR SCREW SYSTEMMarch 1, 2004
K024233KOMPRESSOR SCREW SYSTEMFebruary 6, 2003
K030037UNIVERSAL TOTAL WRIST SYSTEMFebruary 5, 2003
K023770K2 HEMI TOE IMPLANT SYSTEM (FORMERLY ZOBEL GREAT TOE IMPLANT SYSTEM)December 12, 2002
K020554MODIFICATION TO UNIVERSAL TOTAL WRIST SYSTEMMay 3, 2002
K991873KMI WRIST FUSION SYSTEMAugust 17, 1999
K990094KMI WRIST FUSION SYSTEMFebruary 18, 1999
K960539DIAO HAND SURGERY SETJuly 23, 1996
K960692SUBTALAR MBA SYSTEMJuly 23, 1996
K961051UNIVERSAL TOTAL WRIST SYSTEM (MODIFICATION)June 6, 1996
K960533K3 BONE SCREW SYSTEMMarch 25, 1996
K960537K2 BONE SCREW SYSTEMMarch 25, 1996
K950704K4 BONE SCREW SYSTEMJune 30, 1995
K924724KINETIK GREAT TOE SYSTEMJanuary 5, 1994