Class Class II

Arthrex SpeedFLEX™ Implant (K251690)

K251690 2025-09-30 Traditional
Home/ Devices/ Arthrex SpeedFLEX™ Implant (K251690)

Description

Arthrex SpeedFLEX™ Implant by Arthrex, Inc., an FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251690
Clearance Date2025-09-30
Clearance TypeTraditional
Product CodeOWY
Regulation Number878.3300

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