K-number	K130217
Device name	ORTHOPEDIATRICS ACL RECONSTRUCTIVE SYSTEM
Applicant	OrthoPediatrics Corp.
Product code	MBI
Device class	Class II
Decision date	Jun 20, 2013
Decision	Substantially Equivalent
Regulation	888.3040

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Source

View the full FDA submission: accessdata.fda.gov

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ORTHOPEDIATRICS ACL RECONSTRUCTIVE SYSTEM

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