| 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 | PORT-A-CATH EPIDURAL IMPLANTABLE ACCESS SYSTEM |
| Generic Name | CATHETER, PERCUTANEOUS, LONG TERM, INTRASPINAL |
| Applicant | Smiths Medical Asd, Inc. 1265 Grey Fox Rd. St. Paul, MN 55112 |
| PMA Number | P900052 |
| Supplement Number | S010 |
| Date Received | 10/31/2001 |
| Decision Date | 06/11/2002 |
| Withdrawal Date | 12/26/2018 |
| Product Code |
LNY |
| Advisory Committee |
General Hospital |
| 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 THE MANUFACTURING FACILITY LOCATED AT THE FINISHING/POLISHING FACILITY LOCATED AT ELTRONIC, COON RAPIDS, MINNESOTA. |
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