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FDA 510(k) Applications Submitted by IMEDICOM Co., Ltd.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K150915
04/06/2015
SPINAUT-P
IMEDICOM CO., LTD.
K151268
05/13/2015
SPINAUT-V, SPINAUT-S, SPINAUT-I
IMEDICOM CO., LTD.
K182287
08/23/2018
MEDINAUT Plus
Imedicom Co., Ltd.
K153296
11/13/2015
MEDINAUT Kyphoplasty System
IMEDICOM Co., Ltd.
K150789
03/25/2015
SPINAUT-E, SPINAUT-I
IMEDICOM CO., LTD.
K173541
11/15/2017
EPINAUT
Imedicom Co., Ltd.
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