K-number	K240856
Device name	Hip Spacer Molds; Knee Spacer Molds; Shoulder Spacer Molds
Applicant	Osartis GmbH
Product code	MBB
Device class	Class II
Decision date	Nov 20, 2024
Decision	Substantially Equivalent
Regulation	888.3027

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Source

View the full FDA submission: accessdata.fda.gov

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Hip Spacer Molds; Knee Spacer Molds; Shoulder Spacer Molds

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