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FDA 510(k), K173143, Phasix ST Mesh
FDA 510(k), K173143, Phasix ST Mesh
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510(K) Number: K173143
Device Name: Phasix ST Mesh
Manufacturer: C. R. Bard Inc
Device Classification Name: mesh, surgical, absorbable, abdominal hernia
Regulation Number: 878.3300
Classification Product Code: OWT
Date Received: 09/29/2017
Decision Date: 04/25/2018
Regulation Medical Specialty: General & Plastic Surgery
Device Name: Phasix ST Mesh
Manufacturer: C. R. Bard Inc
Device Classification Name: mesh, surgical, absorbable, abdominal hernia
Regulation Number: 878.3300
Classification Product Code: OWT
Date Received: 09/29/2017
Decision Date: 04/25/2018
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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