PMA P860005S002
- Device
- INTERPORE PRO OSTEAN(R)IMPLANT 500 COR. HYDROX
- Applicant
- Interpore Intl.
- PMA number
- P860005
- Supplement
- S002
- Product code
- MBS
- Decision date
- 1993-11-17
- Generic name
- Filler, bone void, non-osteoinduction
Current openFDA PMA Record#
- Device
- INTERPORE PRO OSTEAN(R)IMPLANT 500 COR. HYDROX
- Applicant
- Interpore Intl.
- PMA number
- P860005
- Supplement
- S002
- Product code
- MBS
- Generic name
- Filler, bone void, non-osteoinduction
- Decision date
- 1993-11-17
- Decision code
- APPR
- Date received
- 1993-03-23
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material