K-number	K955914
Device name	LIMITED REUSE ARTHROSCOPIC BLADES
Applicant	Smith & Nephew Dyonics, Inc.
Product code	HRX
Device class	Class II
Decision date	Feb 8, 1996
Decision	Substantially Equivalent
Regulation	888.1100

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View the full FDA submission: accessdata.fda.gov

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LIMITED REUSE ARTHROSCOPIC BLADES

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