Class Class II

Allomatrix (Allomatrix Injectable Putty; Allomatrix C; Allomatrix DR; Allomatrix Custom) (K252085)

K252085 2025-09-30 Traditional
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Description

Allomatrix (Allomatrix Injectable Putty; Allomatrix C; Allomatrix DR; Allomatrix Custom) by Wright Medical Technology, Inc. (Stryker Corporation), an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252085
Clearance Date2025-09-30
Clearance TypeTraditional
Product CodeMQV
Regulation Number888.3045

Categories

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