ANAXBLEND MODEL 20XXX (SEVERAL), ANAXGUM MODEL 25XXX (U), MOCK-UP DIRECT MODEL 240XXX (U), MOCK-UP DIRECT FLOW MODEL 24A (K112044) — FDA 510(k) Clearance | Predicase

K-number	K112044
Device name	ANAXBLEND MODEL 20XXX (SEVERAL), ANAXGUM MODEL 25XXX (U), MOCK-UP DIRECT MODEL 240XXX (U), MOCK-UP DIRECT FLOW MODEL 24A
Applicant	Anaxdent GmbH
Product code	EBF
Device class	Class II
Decision date	Jan 26, 2012
Decision	Substantially Equivalent
Regulation	872.3690

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View the full FDA submission: accessdata.fda.gov

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