Class Class II

My3D® Personalized Pelvic Reconstruction (K223348)

K223348 2023-01-30 Traditional
Home/ Devices/ My3D® Personalized Pelvic Reconstruction…

Description

My3D® Personalized Pelvic Reconstruction by Onkos Surgical, Inc. — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223348
Clearance Date2023-01-30
Clearance TypeTraditional
Product CodeLPH
Regulation Number888.3358

Categories

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top