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Shanghai Iatrical-Ti Technologies CO , Ltd.

FDA 510(k) & PMA Approved Devices — 1 products

Total Devices1
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K232996 Iatrical Interbody Lumbar Fusion Systems (Model ALIF, Model TLIF, Model LLIF)MAX2024-09-06 View
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