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FDA 510(k), K900138, MOTECH TITANIUM SURGICAL MESH
FDA 510(k), K900138, MOTECH TITANIUM SURGICAL MESH
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510(K) Number: K900138
Device Name: MOTECH TITANIUM SURGICAL MESH
Manufacturer: BIEDERMANN MOTECH GMBH
Device Classification Name: mesh, surgical, metal
Regulation Number: 878.3300
Classification Product Code: EZX
Date Received: 01/11/1990
Decision Date: 03/20/1990
Regulation Medical Specialty: General & Plastic Surgery
Device Name: MOTECH TITANIUM SURGICAL MESH
Manufacturer: BIEDERMANN MOTECH GMBH
Device Classification Name: mesh, surgical, metal
Regulation Number: 878.3300
Classification Product Code: EZX
Date Received: 01/11/1990
Decision Date: 03/20/1990
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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