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FDA 510(k), K013672, BRUGES DISTRACTION - ANCHORING - OSTEOSYNTHESIS SYSTEM
FDA 510(k), K013672, BRUGES DISTRACTION - ANCHORING - OSTEOSYNTHESIS SYSTEM
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510(K) Number: K013672
Device Name: BRUGES DISTRACTION - ANCHORING - OSTEOSYNTHESIS SYSTEM
Manufacturer: AZARY TECHNOLOGIES LLC.
Device Classification Name: Plate, Bone
Regulation Number: 872.4760
Classification Product Code: JEY
Date Received: 11/06/2001
Decision Date: 04/08/2002
Regulation Medical Specialty: Dental
Device Name: BRUGES DISTRACTION - ANCHORING - OSTEOSYNTHESIS SYSTEM
Manufacturer: AZARY TECHNOLOGIES LLC.
Device Classification Name: Plate, Bone
Regulation Number: 872.4760
Classification Product Code: JEY
Date Received: 11/06/2001
Decision Date: 04/08/2002
Regulation Medical Specialty: Dental
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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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