GENESIS DUAL 4-CHANNEL IMPLANTABLE PULSE GENERATOR (IPG)
FDA premarket approval P010032/S016 · decided 2005-05-05
Approval details
- PMA number
- P010032
- Supplement
- S016
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- GENESIS DUAL 4-CHANNEL IMPLANTABLE PULSE GENERATOR (IPG)
- Generic name
- Stimulator, spinal-cord, totally implanted for pain relief
- Applicant
- ABBOTT MEDICAL
- Date received
- 2005-02-22
- Decision date
- 2005-05-05
- Days to decision
- 72 days
- Decision code
- APPR
- Product code
- LGW
- Advisory committee
- Neurology
- Expedited review
- No
- Location
- Plano, TX
- Statement
- APPROVAL FOR THE GENESIS DUAL 4-CHANNEL IMPLANTABLE PULSE GENERATOR (IPG), MODEL 3643 WHICH IS INDICATED AS AN AID IN THE MANAGEMENT OF CHRONIC INTRACTABLE PAIN OF THE TRUNK AND/OR LIMBS, INCLUDING UNILATERAL OR BILATERAL PAIN ASSOCIATED WITH FAILED BACK SURGERY SYNDROME, INTRACTABLE LOW BACK PAIN AND LEG PAIN.
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