PATHWAY MODEL 07XXXX (K111774) — FDA 510(k) Clearance | Predicase

K-number	K111774
Device name	PATHWAY MODEL 07XXXX
Applicant	Custom Spine
Product code	MAX
Device class	Class II
Decision date	Jul 20, 2011
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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