Axium Clinical and Patient Programmers
FDA premarket approval P150004/S016 · decided 2017-12-08
Approval details
- PMA number
- P150004
- Supplement
- S016
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Axium Clinical and Patient Programmers
- Generic name
- Dorsal root ganglion stimulator for pain relief
- Applicant
- ABBOTT MEDICAL
- Date received
- 2017-11-09
- Decision date
- 2017-12-08
- Days to decision
- 29 days
- Decision code
- OK30
- Product code
- PMP
- Advisory committee
- Neurology
- Expedited review
- No
- Location
- Plano, TX
- Statement
- Addition of a recharging process for the Axium Patient and Clinical Programmer at the Plano, Texas manufacturing facility to maintain battery level while the programmers are in inventory.
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