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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 8 of 8 Results
510(K) Number: K041669
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Product Description
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Recall
Class
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FDA Recall
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Peri-Strips Dry with Veritas Collagen Matrix Staple Line Reinforcement (PSDV), sterile EO, Rx Only, ... 3 11/23/2011 Synovis Surgical Inovation Div. of
Synovis Peri-Strips Dry with Veritas Collagen Matrix Circular Staple Line Reinforcement, (PSD 25-E-V... 2 06/15/2007 Synovis Surgical Inovation Div. of
Synovis Peri-Strips Dry with Veritas Collagen Matrix Circular Staple Line Reinforcement,( PSD 21-E-V... 2 06/15/2007 Synovis Surgical Inovation Div. of
Synovis Peri-Strips Dry with Veritas Collagen Matrix Circular Staple Line Reinforcement, ( PSD 29-E-... 2 06/15/2007 Synovis Surgical Inovation Div. of
Synovis Peri-Strips Dry with Veritas Collagen Matrix Circular Staple Line Reinforcement, ( PSD 21-U-... 2 06/15/2007 Synovis Surgical Inovation Div. of
Synovis Peri-Strips Dry with Veritas Collagen Matrix Circular Staple Line Reinforcement, ( PSD 25-U-... 2 06/15/2007 Synovis Surgical Inovation Div. of
Synovis Peri-Strips Dry with Veritas Collagen Matrix Circular Staple Line Reinforcement, (PSD 28-U-V... 2 06/15/2007 Synovis Surgical Inovation Div. of
Peri-Strips Dry with Veritas Collagen Matrix Circular Staple Line Reinforcement. Do not reuse. Eth... 2 04/13/2006 Synovis Surgical Inovation Div. of
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