K-number	K861576
Device name	SHORTENING OSTEOTOMY GUIDE
Applicant	Osteotomy Guide Co.
Product code	HTH
Device class	Class I
Decision date	May 12, 1986
Decision	Substantially Equivalent
Regulation	888.4600

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View the full FDA submission: accessdata.fda.gov

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SHORTENING OSTEOTOMY GUIDE

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