Class Class II

TECHFIT Patient-Specific Cranial System (K250297)

K250297 2025-10-27 Traditional
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Description

TECHFIT Patient-Specific Cranial System by Techfit Digital Surgery, Inc., an FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250297
Clearance Date2025-10-27
Clearance TypeTraditional
Product CodeGWO
Regulation Number882.5320

Categories

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