Class Class II

AltiVate Reverse® ADLC Glenosphere (K252567)

K252567 2026-01-15 Traditional
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Description

AltiVate Reverse® ADLC Glenosphere by Encore Medical, L.P., an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252567
Clearance Date2026-01-15
Clearance TypeTraditional
Product CodePHX
Regulation Number888.3660

Categories

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