China NMPA Product Recall - Ogival Interbody interbody fusion device
China NMPA product recall for Ogival Interbody interbody fusion device by Stryker Spine Corporation published June 01, 2023. Recall level: Level 3 Recall. Stryker Spine Corporation, through its Beijing subsidiary Stryker (Beijing) Medical Devices Co., Ltd
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China NMPA product recall for Ogival Interbody interbody fusion device by Stryker Spine Corporation published June 01, 2023. Recall level: Level 3 Recall. Stryker Spine Corporation, through its Beijing subsidiary Stryker (Beijing) Medical Devices Co., Ltd
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Company
Stryker Spine CorporationInspection Date
Unknown Date
Product Type
ID: 0737c60d-547f-4c52-a2f0-96308f8e6e38
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