| 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 | ROTABLATOR ROTATIONAL ANGIOPLASTY SYSTEM CONTRACT STERILIZER |
| Generic Name | CATHETER, CORONARY, ATHERECTOMY |
| Applicant | Boston Scientific Corp Two Scimed Pl. Maple Grove, MN 55311 |
| PMA Number | P900056 |
| Supplement Number | S023 |
| Date Received | 01/30/1998 |
| Decision Date | 02/23/1998 |
| Product Code |
MCX |
| Advisory Committee |
Cardiovascular |
| Supplement Type | Normal 180 Day Track |
| Supplement Reason | Location Change - Manufacturer/Sterilizer/Packager/Supplier |
| Expedited Review Granted? | No |
| Combination Product | No |
| Predetermined Change Control Plan Authorized | No |
Approval Order Statement Approval for an alternate contract sterilizer at Griffith Micro Science, New York facility, 84 Park Road, Queensbury, NY 12804. |
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