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U.S. Department of Health and Human Services

510(k) Premarket Notification

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51 to 60 of 500 Results *
Decision Date To: 07/22/2019
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510(K)
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advanced intermezzo implant system MegaGen Implant Co., Ltd. K191127 10/08/2019
premia spine xl instruments Premia Spine, Ltd. K191854 10/08/2019
barrier sleeves Ivoclar Vivadent, AG K191448 10/08/2019
single-use non-stick bipolar forceps bayonet, single-use non-stick bipolar irrigating forceps, single use non-stick bipolar suction forceps Faulhaber Pinzetten OHG K182773 10/08/2019
tsolution one total knee application THINK Surgical, Inc. K191369 10/08/2019
bodycad unicompartmental knee system Bodycad Laboratories, Inc. K191150 10/08/2019
attune revision lps inserts Depuy (Ireland) K191779 10/08/2019
scopeseal duodenoscope protective device GI Scientific LLC K183171 10/08/2019
katana cleaner, katana cleaner (trial) Kuraray Noritake Dental Inc. K191133 10/08/2019
nio-i WaisMed Ltd K190538 10/07/2019

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
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