Class Class II

Mako Total Knee Application (3.0); Hybrid Tip Pointer (K250608)

K250608 2025-04-25 Traditional
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Description

Mako Total Knee Application (3.0); Hybrid Tip Pointer by Mako Surgical Corp., an FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250608
Clearance Date2025-04-25
Clearance TypeTraditional
Product CodeOLO
Regulation Number882.4560

Categories

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