K-number	K855224
Device name	ACROMED NESTED BONE PLATE
Applicant	Buckman Co., Inc.
Product code	JEY
Device class	Class II
Decision date	Feb 4, 1986
Decision	Substantially Equivalent
Regulation	872.4760

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View the full FDA submission: accessdata.fda.gov

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ACROMED NESTED BONE PLATE

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