K-number	K960852
Device name	HALL MODULAR ACETABULAR REAMER SYSTEM
Applicant	Linvatec Corp.
Product code	HWE
Device class	Class I
Decision date	Mar 20, 1996
Decision	Substantially Equivalent
Regulation	878.4820

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View the full FDA submission: accessdata.fda.gov

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HALL MODULAR ACETABULAR REAMER SYSTEM

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