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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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