K-number	K133367
Device name	ORTHOVIS PREOPERATIVE PLAN
Applicant	Custom Orthopaedic Solutions
Product code	LLZ
Device class	Class II
Decision date	Dec 20, 2013
Decision	Substantially Equivalent
Regulation	892.2050

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Source

View the full FDA submission: accessdata.fda.gov

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ORTHOVIS PREOPERATIVE PLAN

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