Class Class II

OSSIOfiber® Compression Staple (K241932)

K241932 2024-08-28 Traditional
Home/ Devices/ OSSIOfiber® Compression Staple (K241932)

Description

OSSIOfiber® Compression Staple by OSSIO , Ltd. — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK241932
Clearance Date2024-08-28
Clearance TypeTraditional
Product CodeMNU
Regulation Number888.3030

Categories

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