Class Class II

Citregen™ Tendon Interference Screw (TIS), Citrelock™ Tendon Fixation Device, Citrespline™ and Citrelock™ ACL Implants (K221468)

K221468 2023-02-14 Traditional
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Description

Citregen™ Tendon Interference Screw (TIS), Citrelock™ Tendon Fixation Device, Citrespline™ and Citrelock™ ACL Implants by Acuitive Technologies, Inc. — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK221468
Clearance Date2023-02-14
Clearance TypeTraditional
Product CodeMAI
Regulation Number888.3030

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