Class Class II

RFG-01 (K240178)

K240178 2024-07-15 Traditional
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Description

RFG-01 by Zimmer Medizinsysteme GmbH — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK240178
Clearance Date2024-07-15
Clearance TypeTraditional
Product CodePBX
Regulation Number878.4400

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