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FDA 510(k), K152304, Tritanium PL Cage
FDA 510(k), K152304, Tritanium PL Cage
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$149.00 USD
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510(K) Number: K152304
Device Name: Tritanium PL Cage
Manufacturer: Stryker
Device Classification Name: intervertebral fusion device with bone graft, lumbar
Regulation Number: 888.3080
Classification Product Code: MAX
Date Received: 08/14/2015
Decision Date: 11/19/2015
Regulation Medical Specialty: Orthopedic
Device Name: Tritanium PL Cage
Manufacturer: Stryker
Device Classification Name: intervertebral fusion device with bone graft, lumbar
Regulation Number: 888.3080
Classification Product Code: MAX
Date Received: 08/14/2015
Decision Date: 11/19/2015
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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