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Product Description
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Recall Class
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FDA Recall Posting Date
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Recalling Firm
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Z-1383-2016 - SYNTHECEL Dura Repair, 510K # K131792, K113071, Class II, Classification name: Dura Substitute
Device listing number: D140596, D211012
SYNTHECEL Dura Repair is intended for use as a dura replacement...
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2
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10/11/2018
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Synthes (USA) Products LLC
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Z-1384-2016 - SYNTHECEL Dura Repair, 510K # K131792, K113071, Class II, Classification name: Dura Substitute
Device listing number: D140596, D211012
SYNTHECEL Dura Repair is intended for use as a dura replacement...
|
2
|
10/11/2018
|
Synthes (USA) Products LLC
|
Z-1387-2016 - SYNTHECEL Dura Repair, 510K # K131792, K113071, Class II, Classification name: Dura Substitute
Device listing number: D140596, D211012
SYNTHECEL Dura Repair is intended for use as a dura replacement...
|
2
|
10/11/2018
|
Synthes (USA) Products LLC
|
Z-1386-2016 - SYNTHECEL Dura Repair, 510K # K131792, K113071, Class II, Classification name: Dura Substitute
Device listing number: D140596, D211012
SYNTHECEL Dura Repair is intended for use as a dura replacement...
|
2
|
10/11/2018
|
Synthes (USA) Products LLC
|
Z-1385-2016 - SYNTHECEL Dura Repair, 510K # K131792, K113071, Class II, Classification name: Dura Substitute
Device listing number: D140596, D211012
SYNTHECEL Dura Repair is intended for use as a dura replacement...
|
2
|
10/11/2018
|
Synthes (USA) Products LLC
|