K-number	K992348
Device name	SYNTHES SPIRAL BLADE FOR HUMERAL NAIL (SBHN)
Applicant	Synthes (Usa)
Product code	JDS
Device class	Class II
Decision date	Sep 23, 1999
Decision	Substantially Equivalent
Regulation	888.3030

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View the full FDA submission: accessdata.fda.gov

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SYNTHES SPIRAL BLADE FOR HUMERAL NAIL (SBHN)

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