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FDA 510(k), K973924, FRIOS BONESHIELD
FDA 510(k), K973924, FRIOS BONESHIELD
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510(K) Number: K973924
Device Name: FRIOS BONESHIELD
Manufacturer: FRIATEC AG
Device Classification Name: plate, bone
Regulation Number: 872.4760
Classification Product Code: JEY
Date Received: 10/15/1997
Decision Date: 05/07/1998
Regulation Medical Specialty: Dental
Device Name: FRIOS BONESHIELD
Manufacturer: FRIATEC AG
Device Classification Name: plate, bone
Regulation Number: 872.4760
Classification Product Code: JEY
Date Received: 10/15/1997
Decision Date: 05/07/1998
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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