K-number	K837776
Device name	AOR X-RAY ALIGMENT PAD
Applicant	Zimmer, Inc.
Product code	IXJ
Device class	Class I
Decision date	Aug 18, 1983
Decision	Substantially Equivalent
Regulation	892.1910

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View the full FDA submission: accessdata.fda.gov

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AOR X-RAY ALIGMENT PAD

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