K-number	K230540
Device name	Patient Specific Planning Solution 3D Bone Models
Applicant	Biomet Manufacturing Corp
Product code	LLZ
Device class	Class II
Decision date	Jul 25, 2023
Decision	Substantially Equivalent
Regulation	892.2050

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Source

View the full FDA submission: accessdata.fda.gov

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Patient Specific Planning Solution 3D Bone Models

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Patient Specific Planning Solution 3D Bone Models