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FDA 510(k), K171173, OrthoPediatrics Titanium PediPlates® System
FDA 510(k), K171173, OrthoPediatrics Titanium PediPlates® System
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510(K) Number: K171173
Device Name: OrthoPediatrics Titanium PediPlates® System
Manufacturer: OrthoPediatrics, Corp.
Device Classification Name: plate, fixation, bone
Regulation Number: 888.3030
Classification Product Code: HRS
Date Received: 04/21/2017
Decision Date: 08/24/2017
Regulation Medical Specialty: Orthopedic
Device Name: OrthoPediatrics Titanium PediPlates® System
Manufacturer: OrthoPediatrics, Corp.
Device Classification Name: plate, fixation, bone
Regulation Number: 888.3030
Classification Product Code: HRS
Date Received: 04/21/2017
Decision Date: 08/24/2017
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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