Medical Device Safety and Recalls: Stryker Spine - OASYS Midline Occiput Plate

You are subscribed to receive updates about Medical Device Safety and Recalls for the U.S. Food & Drug Administration (FDA). Information about the Stryker Spine - OASYS Midline Occiput Plate Class I Recall has recently been posted. Manage your FDA Subscriptions: Update your preferences or unsubscribe Questions about this service? support@govdelivery.com Other inquiries? webmail@oc.fda.gov This email was sent to kostikblog@ukr.net using GovDelivery, on behalf of: U.S. Food & Drug Administration (FDA) · 10903 New Hampshire Ave · Silver Spring, MD 20993 · 800-439-1420