K-number	K954915
Device name	FLEXIBLE INTRAMEDULLARY REAMER
Applicant	Zimmer, Inc.
Product code	HTO
Device class	Class I
Decision date	Dec 28, 1995
Decision	Substantially Equivalent
Regulation	888.4540

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View the full FDA submission: accessdata.fda.gov

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FLEXIBLE INTRAMEDULLARY REAMER

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