Stimulator, spinal-cord, totally implanted for pain relief
PMA 核准號：P840001 · 2026-09-24
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器材摘要
Stimulator, spinal-cord, totally implanted for pain relief is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Neuromodulation. It received FDA 510(k) clearance on 2026-09-24. The device is classified under product code LGW. It was reviewed by the NE advisory panel.
常見問題
What is the Stimulator, spinal-cord, totally implanted for pain relief?
Stimulator, spinal-cord, totally implanted for pain relief is a medical device that received FDA 510(k) clearance on 2026-09-24. The listed applicant is Medtronic Neuromodulation.
When did Stimulator, spinal-cord, totally implanted for pain relief receive FDA 510(k) clearance?
The clearance date for Stimulator, spinal-cord, totally implanted for pain relief can be found in the official FDA records.
Who is the listed applicant for Stimulator, spinal-cord, totally implanted for pain relief?
The FDA 510(k) record lists Medtronic Neuromodulation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Stimulator, spinal-cord, totally implanted for pain relief?
The FDA product code for Stimulator, spinal-cord, totally implanted for pain relief is LGW.
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官方來源
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