FDA 510(k) Applications Submitted by ALTIVA CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K070891 03/30/2007 ALTIVA CLASSIC ACP SYSTEM ALTIVA CORP.
K051216 05/12/2005 HYDRALOK SYSTEM ALTIVA CORP.
K061482 05/30/2006 ALTES BUTTRESS PLATING SYSTEM ALTIVA CORP.
K051044 04/25/2005 ARCTEC SEMIRIGID PLATING SYSTEM ALTIVA CORP.
K053070 11/01/2005 CONTOUR II SPINAL SYSTEM ALTIVA CORP.


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