K-number	K203634
Device name	BioPoly Great Toe Hemiarthroplasty Implant
Applicant	BioPoly, LLC
Product code	KWD
Device class	Class II
Decision date	Feb 2, 2021
Decision	Substantially Equivalent
Regulation	888.3730

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Source

View the full FDA submission: accessdata.fda.gov

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BioPoly Great Toe Hemiarthroplasty Implant

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