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FDA 510(k), K162770, Relign System
FDA 510(k), K162770, Relign System
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$149.00 USD
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510(K) Number: K162770
Device Name: Relign System
Manufacturer: Relign Corporation
Device Classification Name: Electrosurgical, Cutting & Coagulation & Accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 10/03/2016
Decision Date: 01/04/2017
Regulation Medical Specialty: General & Plastic Surgery
Device Name: Relign System
Manufacturer: Relign Corporation
Device Classification Name: Electrosurgical, Cutting & Coagulation & Accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 10/03/2016
Decision Date: 01/04/2017
Regulation Medical Specialty: General & Plastic Surgery
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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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