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FDA 510(k), K160959, Xsert Lumbar Expandable Interbody System
FDA 510(k), K160959, Xsert Lumbar Expandable Interbody System
Regular price
$149.00 USD
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$149.00 USD
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510(K) Number: K160959
Device Name: Xsert Lumbar Expandable Interbody System
Manufacturer: X-SPINE SYSTEMS, INC.
Device Classification Name: intervertebral fusion device with bone graft, lumbar
Regulation Number: 888.3080
Classification Product Code: MAX
Date Received: 04/05/2016
Decision Date: 11/17/2016
Regulation Medical Specialty: Orthopedic
Device Name: Xsert Lumbar Expandable Interbody System
Manufacturer: X-SPINE SYSTEMS, INC.
Device Classification Name: intervertebral fusion device with bone graft, lumbar
Regulation Number: 888.3080
Classification Product Code: MAX
Date Received: 04/05/2016
Decision Date: 11/17/2016
Regulation Medical Specialty: Orthopedic
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