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FDA 510(k), K021736, BARD VENTRALEX HERNIA PATCH, MODELS 0010302, 0010301
FDA 510(k), K021736, BARD VENTRALEX HERNIA PATCH, MODELS 0010302, 0010301
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510(K) Number: K021736
Device Name: BARD VENTRALEX HERNIA PATCH, MODELS 0010302, 0010301
Manufacturer: C.R. BARD, INC.
Device Classification Name: mesh, surgical, polymeric
Regulation Number: 878.3300
Classification Product Code: FTL
Date Received: 05/28/2002
Decision Date: 07/16/2002
Regulation Medical Specialty: General & Plastic Surgery
Device Name: BARD VENTRALEX HERNIA PATCH, MODELS 0010302, 0010301
Manufacturer: C.R. BARD, INC.
Device Classification Name: mesh, surgical, polymeric
Regulation Number: 878.3300
Classification Product Code: FTL
Date Received: 05/28/2002
Decision Date: 07/16/2002
Regulation Medical Specialty: General & Plastic Surgery
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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