FDA 510(k) Applications Submitted by SKELETAL KINETICS, LLC
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K120354 |
02/06/2012 |
BETA-TCP GRANULES |
SKELETAL KINETICS, LLC |
K100986 |
04/09/2010 |
CALLOS BONE VOID FILLER, SKAFFOLD NEXT GENERATION BONE VOID FILLER, OSTEO VATION |
SKELETAL KINETICS, LLC |
K111538 |
06/02/2011 |
SKAFFOLD CIS |
SKELETAL KINETICS, LLC |
K132211 |
07/16/2013 |
SKAFFOLD NMX BONE VOID FILLER |
SKELETAL KINETICS, LLC |
K112383 |
08/18/2011 |
CALLOS PROMODEL BONE VOID FILLER, SKAFFOLD MP (MACRO POROUS) BONE VOID FILLER |
SKELETAL KINETICS, LLC |
K051123 |
05/03/2005 |
CALLOS IMPACT AND INJECT BONE VOID FILLER |
SKELETAL KINETICS, LLC |
K051784 |
07/01/2005 |
OSTEOVATION CMF BONE VOID FILLER |
SKELETAL KINETICS, LLC |
K042072 |
08/02/2004 |
CALLOS CMF BONE VOID FILLER |
SKELETAL KINETICS, LLC |
K030554 |
02/21/2003 |
CALLOS |
SKELETAL KINETICS, LLC |
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