PMA P860005S007

Device
PRO OSTEON IMPLANT 500 CORALLINE HYDROXYPATITE BONE VOID FILLER (FORMERLY INTERPORE 500)
Applicant
Interpore Intl.
PMA number
P860005
Supplement
S007
Product code
MBS
Decision date
1997-05-30
Generic name
Filler, bone void, non-osteoinduction
Approval order statement
APPROVAL FOR A MANUFACTURING SITE LOCATED AT STERIGENICS, INTERNATIONAL, 344 BONNIE CIRCLE, CORONA, CA.

Current openFDA PMA Record#

Device
PRO OSTEON IMPLANT 500 CORALLINE HYDROXYPATITE BONE VOID FILLER (FORMERLY INTERPORE 500)
Applicant
Interpore Intl.
PMA number
P860005
Supplement
S007
Product code
MBS
Generic name
Filler, bone void, non-osteoinduction
Decision date
1997-05-30
Decision code
APPR
Date received
1997-05-15
Supplement type
Normal 180 Day Track
Supplement reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
APPROVAL FOR A MANUFACTURING SITE LOCATED AT STERIGENICS, INTERNATIONAL, 344 BONNIE CIRCLE, CORONA, CA.