China NMPA Product Recall - Interbody fusion device
China NMPA product recall for Interbody fusion device by NuVasive Inc. (USA) published January 24, 2019. Recall level: Level 3 Recall. NuVasive Inc. (USA) has initiated a voluntary Class III recall of its interbody fusion devices (Nati
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China NMPA product recall for Interbody fusion device by NuVasive Inc. (USA) published January 24, 2019. Recall level: Level 3 Recall. NuVasive Inc. (USA) has initiated a voluntary Class III recall of its interbody fusion devices (Nati
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Company
NuVasive Inc. (USA)Inspection Date
Unknown Date
Product Type
ID: 10930398-58ec-4dd7-9ef8-fe4c28c2505e
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