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FDA 510(k), K151068, SureLock W Suture Anchor
FDA 510(k), K151068, SureLock W Suture Anchor
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510(K) Number: K151068
Device Name: SureLock W Suture Anchor
Manufacturer: CAYENNE MEDICAL, INC
Device Classification Name: fastener, fixation, nondegradable, soft tissue
Regulation Number: 888.3040
Classification Product Code: MBI
Date Received: 04/21/2015
Decision Date: 07/24/2015
Regulation Medical Specialty: Orthopedic
Device Name: SureLock W Suture Anchor
Manufacturer: CAYENNE MEDICAL, INC
Device Classification Name: fastener, fixation, nondegradable, soft tissue
Regulation Number: 888.3040
Classification Product Code: MBI
Date Received: 04/21/2015
Decision Date: 07/24/2015
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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