K-number	K882831
Device name	ACE CANCELLOUS BONE SCREW
Applicant	Buckman Co., Inc.
Product code	HWC
Device class	Class II
Decision date	Aug 1, 1988
Decision	Substantially Equivalent
Regulation	888.3040

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View the full FDA submission: accessdata.fda.gov

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ACE CANCELLOUS BONE SCREW

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