Class Class

Remanufactured EndoWrist Cadiere Forceps (420049) (K250399)

K250399 2025-08-19 Traditional
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Description

Remanufactured EndoWrist Cadiere Forceps (420049) by Rebotix, an FDA 510(k) cleared unknown device.

Regulatory Information

Device ClassClass Class
510(k) NumberK250399
Clearance Date2025-08-19
Clearance TypeTraditional

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