GENESIS AND EON FAMILY NEUROSTIMULATION (IPG) SYSTEMS
FDA premarket approval P010032/S050 · decided 2013-06-26
Approval details
- PMA number
- P010032
- Supplement
- S050
- Supplement type
- 135 Review Track For 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- GENESIS AND EON FAMILY NEUROSTIMULATION (IPG) SYSTEMS
- Generic name
- Stimulator, spinal-cord, totally implanted for pain relief
- Applicant
- ABBOTT MEDICAL
- Date received
- 2012-04-18
- Decision date
- 2013-06-26
- Days to decision
- 434 days
- Decision code
- APPR
- Product code
- LGW
- Advisory committee
- Neurology
- Expedited review
- No
- Location
- Plano, TX
- Statement
- APPROVAL FOR THE ADDITION OF SEVERAL PIECES OF EQUIPMENT THAT ARE NEW TO THE MANUFACTURING PROCESS AS WELL AS THE RELOCATION OF EQUIPMENT AND THE ADDITION OF AN ALREADY APPROVED PIECE OF EQUIPMENT TO THE BILBY ROAD FACILITY LOCATION.
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510(k) clearances by this applicant
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|---|---|---|
| EnSite™ X EP System (K262006) | Abbott Medical | 2026-07-15 |
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| OPTIS Mobile Next Imaging System (1014932); OPTIS Integrated Next Imaging System (1014933); Ultreon 3.0 Software Upgrade Kit (ULTR300001) (K253459) | ABBOTT MEDICAL | 2026-04-24 |
| EnSite™ X EP System (K260212) | ABBOTT MEDICAL | 2026-04-20 |
| Disposable Radiofrequency Cannula (K253907) | ABBOTT MEDICAL | 2026-04-16 |
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| Armada™ 14 NC PTA Catheter (K252512) | ABBOTT MEDICAL | 2026-02-13 |
| Assert-IQ (DM5100) (K253516) | ABBOTT MEDICAL | 2025-12-18 |