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FDA 510(k), K172186, BioWick X Implant with Driver
FDA 510(k), K172186, BioWick X Implant with Driver
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510(K) Number: K172186
Device Name: BioWick X Implant with Driver
Manufacturer: Cayenne Medical, Inc.
Device Classification Name: fastener, fixation, nondegradable, soft tissue
Regulation Number: 888.3040
Classification Product Code: MBI
Date Received: 07/20/2017
Decision Date: 10/16/2017
Regulation Medical Specialty: Orthopedic
Device Name: BioWick X Implant with Driver
Manufacturer: Cayenne Medical, Inc.
Device Classification Name: fastener, fixation, nondegradable, soft tissue
Regulation Number: 888.3040
Classification Product Code: MBI
Date Received: 07/20/2017
Decision Date: 10/16/2017
Regulation Medical Specialty: Orthopedic
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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