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FDA 510(k), K020905, NBX - NON-BRIDGING EXTERNAL FIXATOR
FDA 510(k), K020905, NBX - NON-BRIDGING EXTERNAL FIXATOR
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510(K) Number: K020905
Device Name: NBX - NON-BRIDGING EXTERNAL FIXATOR
Manufacturer: PATRICIA SANDBORN BERES
Device Classification Name: Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite
Regulation Number: LXT
Classification Product Code: 03/20/2002
Date Received: 04/15/2002
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic
Device Name: NBX - NON-BRIDGING EXTERNAL FIXATOR
Manufacturer: PATRICIA SANDBORN BERES
Device Classification Name: Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite
Regulation Number: LXT
Classification Product Code: 03/20/2002
Date Received: 04/15/2002
Decision Date: Substantially Equivalent (SESE)
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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