Note: This medical device record is a PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information. |
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Device | INTERPORE PRO OSTEAN(R)IMPLANT 500 COR. HYDROX |
Generic Name | Filler, bone void, non-osteoinduction |
Applicant | INTERPORE INTL. 181 TECHNOLOGY DR. IRVINE, CA 92618-2402 |
PMA Number | P860005 |
Supplement Number | S003 |
Date Received | 10/15/1993 |
Decision Date | 03/17/1994 |
Reclassified Date
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06/02/2003 |
Product Code |
MBS |
Advisory Committee |
Orthopedic |
Supplement Type | Normal 180 Day Track |
Supplement Reason | Change Design/Components/Specifications/Material |
Expedited Review Granted? | No |
Combination Product | No |
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