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FDA 510(k), K070560, LRTM SURGICAL MESH
FDA 510(k), K070560, LRTM SURGICAL MESH
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$149.00 USD
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510(K) Number: K070560
Device Name: LRTM SURGICAL MESH
Manufacturer: LIFECELL CORP.
Device Classification Name: Mesh, Surgical
Regulation Number: 878.3300
Classification Product Code: FTM
Date Received: 02/27/2007
Decision Date: 06/11/2007
Regulation Medical Specialty: General & Plastic Surgery
Device Name: LRTM SURGICAL MESH
Manufacturer: LIFECELL CORP.
Device Classification Name: Mesh, Surgical
Regulation Number: 878.3300
Classification Product Code: FTM
Date Received: 02/27/2007
Decision Date: 06/11/2007
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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