| Note: this medical device record is a supplement. The device description may have changed. Be sure to look at the Original HDE to get an up-to-date view of this device. |
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| Trade Name | OP-1 IMPLANT |
| Classification Name | filler, recombinant human bone morphogenetic protein, collagen scaffold, osteoinduction |
| Generic Name | filler, recombinant human bone morphogenetic protein, collagen scaffold, osteoinduction |
| Applicant |
| Olympus Biotech Corporation |
| 35 s. st. |
| hopkinton, MA 01748 |
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| HDE Number | H010002 |
| Supplement Number | S017 |
| Date Received | 08/24/2005 |
| Decision Date | 05/02/2008 |
| Product Code | |
| Advisory Committee |
Orthopedic |
| Supplement Type | normal 75 day track |
| Supplement Reason | process change - manufacturer/sterilizer/packager/supplier |
| Expedited Review Granted? | No |
| Combination Product | Yes |
Approval Order Statement Approval for changes in the bioburden tests performed on the bone powder, collagen matrix and pre-irradiated op-i implant, and the deletion of the bioburden resistancespecification for the collagen matrix. |
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