Class Class II

NeuroBlate Fusion-S Software V3.17 (K222983)

K222983 2023-03-15 Traditional
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Description

NeuroBlate Fusion-S Software V3.17 by Monteris Medical, — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK222983
Clearance Date2023-03-15
Clearance TypeTraditional
Product CodeGEX
Regulation Number878.4810

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