K-number	K884161
Device name	ACROMED ILIAC SCREW
Applicant	Buckman Co., Inc.
Product code	KWP
Device class	Class II
Decision date	May 3, 1989
Decision	Substantially Equivalent for Some Indications
Regulation	888.3050

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View the full FDA submission: accessdata.fda.gov

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ACROMED ILIAC SCREW

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