170 results
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44ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PRO OSTEON IMPLANT 500 HYDROXYAPATITE
FDA Adverse Event
Injury
·INTERPORE INTL.·Product code LMN·September 9, 1996
PRO OSTEON IMPLANT 500 CORALLINE HYDROXYAPATITE BONE VOID FI
FDA Adverse Event
Injury
·INTERPORE INTL.·Product code LMN·August 8, 1997
PRO OSTEON IMPLANT 500 BONE VOID FILLER
FDA Adverse Event
Injury
·INTERPORE INTL.·Product code LMN·July 3, 1997
INTERPORE HEX IMPLANT
FDA Adverse Event
Injury
·INTERPORE INTL.·Product code DZE·April 15, 1997
INTERPORE IMZ IMPLANT
FDA Adverse Event
Injury
·INTERPORE INTL.·Product code DZE·April 9, 1997
INTERPORTE IMZ IMPLANT
FDA Adverse Event
Injury
·INTERPORE INTL.·Product code DZE·April 9, 1997
PRO OSTEON IMPLANT 500 CORALLINE HYDROXYAPATITE BONE VOIDE
FDA Adverse Event
Injury
·INTERPORE INTL.·Product code LMN·June 24, 1997
INTERPORE THREADED IMPLANT
FDA Adverse Event
Injury
·INTERPORE INTL.·Product code DZE·April 18, 1997
INTERPORE HEX IMPLANT
FDA Adverse Event
Injury
·INTERPORE INTL.·Product code DZE·April 18, 1997
INTERPORE HEX IMPLANT
FDA Adverse Event
Injury
·INTERPORE INTL.·Product code DZE·April 18, 1997
INTERPORE HEX IMPLANT
FDA Adverse Event
Injury
·INTERPORE INTL.·Product code DZE·April 18, 1997
PRO OSTEON IMPLANT 500 CORALLINE HYDROXYAPATITE BONE VOID FL
FDA Adverse Event
Death
·INTERPORE INTL.·Product code LMN·June 3, 1997
PRO OSTEON IMPLANT 500 CORRALINE HYDROXYAPATITE BONE VOID FI
FDA Adverse Event
Injury
·INTERPORE INTL.·Product code MBP·April 29, 1997
INTERPORE HEX IMPLANT
FDA Adverse Event
Injury
·INTERPORE INTL.·Product code DZE·April 15, 1997
INTERPORE THREADED IMPLANT
FDA Adverse Event
Injury
·INTERPORE INTL.·Product code DZE·April 18, 1997
INTERPORE THREADED IMPLANT
FDA Adverse Event
Injury
·INTERPORE INTL.·Product code DZE·April 18, 1997
INTERPORE IMZ IMPLANT
FDA Adverse Event
Injury
·INTERPORE INTL.·Product code DZE·April 18, 1997
INTERPORE HEX IMPLANT
FDA Adverse Event
Injury
·INTERPORE INTL·Product code DZE·November 5, 1996
INTERPORE IMZ IMPLANT
FDA Adverse Event
Injury
·INTERPORE INTL·Product code DZE·November 5, 1996
INTERPORE IMZ IMPLANT
FDA Adverse Event
Injury
·INTERPORE INTL·Product code DZE·October 10, 1996