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 | MAXUM SYSTEM |
Generic Name | Implant, hearing, active, middle ear, partially implanted |
Applicant | OTOTRONIX, LLC 26620 I-45 NORTH HOUSTON, TX 77386 |
PMA Number | P010023 |
Supplement Number | S003 |
Date Received | 05/18/2010 |
Decision Date | 09/30/2010 |
Product Code |
MPV |
Advisory Committee |
Ear Nose & Throat |
Supplement Type | 135 Review Track For 30-Day Notice |
Supplement Reason | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
Expedited Review Granted? | No |
Combination Product | No |
Approval Order Statement APPROVAL FOR A CHANGE IN THE MAGNET CANISTER MANUFACTURING PROCESS/INSPECTION, AND THE RE-QUALIFICATION OF THE MAGNETIZATION VENDOR AT THE VENDOR¿S NEW FACILITY LOCATION. |
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