Class Class II

Kyphoplasty Balloon System (K221142)

K221142 2023-04-21 Traditional
Home/ Devices/ Kyphoplasty Balloon System (K221142)

Description

Kyphoplasty Balloon System by Ok Medinetkorea Co., Ltd. — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK221142
Clearance Date2023-04-21
Clearance TypeTraditional
Product CodeHRX
Regulation Number888.1100

Categories

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