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FDA 510(k), K150009, Baide
FDA 510(k), K150009, Baide
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$149.00 USD
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510(K) Number: K150009
Device Name: Baide
Manufacturer: Jiangsu Baide Medical Intrument Co.,Ltd.
Device Classification Name: plate, fixation, bone
Regulation Number: 888.3030
Classification Product Code: HRS
Date Received: 01/02/2015
Decision Date: 02/25/2015
Regulation Medical Specialty: Orthopedic
Device Name: Baide
Manufacturer: Jiangsu Baide Medical Intrument Co.,Ltd.
Device Classification Name: plate, fixation, bone
Regulation Number: 888.3030
Classification Product Code: HRS
Date Received: 01/02/2015
Decision Date: 02/25/2015
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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