K-number	K955229
Device name	WRIGHT MEDICAL TECHNOLOGY SAWBLADES
Applicant	Wrightmedicaltechnologyinc
Product code	GFA
Device class	Class I
Decision date	Jan 18, 1996
Decision	Substantially Equivalent
Regulation	878.4820

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Source

View the full FDA submission: accessdata.fda.gov

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WRIGHT MEDICAL TECHNOLOGY SAWBLADES

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