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FDA 510(k), K121289, LTM-LABAROSCOPIC SURGICAL MESH
FDA 510(k), K121289, LTM-LABAROSCOPIC SURGICAL MESH
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510(K) Number: K121289
Device Name: LTM-LABAROSCOPIC SURGICAL MESH
Manufacturer: LIFECELL CORP.
Device Classification Name: Mesh, Surgical, Collagen, Large Abdominal Wall Defects
Regulation Number: 878.3300
Classification Product Code: OXK
Date Received: 04/30/2012
Decision Date: 08/03/2012
Regulation Medical Specialty: General & Plastic Surgery
Device Name: LTM-LABAROSCOPIC SURGICAL MESH
Manufacturer: LIFECELL CORP.
Device Classification Name: Mesh, Surgical, Collagen, Large Abdominal Wall Defects
Regulation Number: 878.3300
Classification Product Code: OXK
Date Received: 04/30/2012
Decision Date: 08/03/2012
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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