VISTA-S DEVICE MODEL 08/06-401-XXXXX, 08/06-402-XXXXXX (K111983) — FDA 510(k) Clearance | Predicase

K-number	K111983
Device name	VISTA-S DEVICE MODEL 08/06-401-XXXXX, 08/06-402-XXXXXX
Applicant	Zimmer Trabecular Metal Technology
Product code	ODP
Device class	Class II
Decision date	Nov 18, 2011
Decision	Substantially Equivalent
Regulation	888.3080

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View the full FDA submission: accessdata.fda.gov

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