脊髓植入式刺激器，用于疼痛缓解
PMA编号：P130028 · 2020-05-05
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决定日期2020-05-05
PMA 编号P130028
产品代码LGW
设备分类第3类
医疗专科U
咨询委员会NE
请注意，您提供的文本“NE”不足以进行翻译，因为它不是一个完整的句子或描述。请提供完整的医疗设备监管文本，以便我能够进行准确的翻译。
器械摘要
Stimulator, spinal-cord, totally implanted for pain relief is the device name listed in this FDA 510(k) record. The listed applicant is Nuvectra Corporation. It received FDA 510(k) clearance on 2020-05-05. The device is classified under product code LGW. It was reviewed by the NE advisory panel.
常见问题
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 2020-05-05. The listed applicant is Nuvectra Corporation.
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.
谁是用于疼痛缓解的完全植入式脊髓刺激器的列名申请人？
The FDA 510(k) record lists Nuvectra Corporation as the applicant. This does not by itself establish the device manufacturer.
什么是用于疼痛缓解的完全植入式脊髓刺激器的FDA产品代码？
FDA产品代码为Stimulator，脊髓植入式，完全植入用于缓解疼痛的是LGW。
相关临床试验
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官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
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