K-number	K130334
Device name	HOFFMANN LRF (LIMB RECONSTRUCTION FRAME SYSTEM)
Applicant	Stryker Trauma AG
Product code	KTT
Device class	Class II
Decision date	May 3, 2013
Decision	Substantially Equivalent
Regulation	888.3030

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View the full FDA submission: accessdata.fda.gov

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HOFFMANN LRF (LIMB RECONSTRUCTION FRAME SYSTEM)

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