Dorsal root ganglion stimulator for pain relief
PMA 核准號：P150004 · 2026-09-23
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器材摘要
Dorsal root ganglion stimulator for pain relief is the device name listed in this FDA 510(k) record. The listed applicant is ABBOTT MEDICAL. It received FDA 510(k) clearance on 2026-09-23. The device is classified under product code PMP. It was reviewed by the NE advisory panel.
常見問題
What is the Dorsal root ganglion stimulator for pain relief?
Dorsal root ganglion stimulator for pain relief is a medical device that received FDA 510(k) clearance on 2026-09-23. The listed applicant is ABBOTT MEDICAL.
When did Dorsal root ganglion stimulator for pain relief receive FDA 510(k) clearance?
The clearance date for Dorsal root ganglion stimulator for pain relief can be found in the official FDA records.
Who is the listed applicant for Dorsal root ganglion stimulator for pain relief?
The FDA 510(k) record lists ABBOTT MEDICAL as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Dorsal root ganglion stimulator for pain relief?
The FDA product code for Dorsal root ganglion stimulator for pain relief is PMP.
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官方來源
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