K-number	K121702
Device name	ORTHOCOR ACTIVE DEVICE ORTHOCOR GENERAL USE ACTIVE DEVICE
Applicant	Orthocor Medical
Product code	ILX
Device class	Class II
Decision date	May 6, 2013
Decision	Substantially Equivalent
Regulation	890.5290

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Source

View the full FDA submission: accessdata.fda.gov

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ORTHOCOR ACTIVE DEVICE ORTHOCOR GENERAL USE ACTIVE DEVICE

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