SMITH & NEPHEW VULCAN ARTICULAR CARTILAGE PROBE, MODEL 721XXXX (K050898) — FDA 510(k) Clearance | Predicase

K-number	K050898
Device name	SMITH & NEPHEW VULCAN ARTICULAR CARTILAGE PROBE, MODEL 721XXXX
Applicant	Smith & Nephew, Inc.
Product code	GEI
Device class	Class II
Decision date	May 25, 2005
Decision	Substantially Equivalent
Regulation	878.4400

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View the full FDA submission: accessdata.fda.gov

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