K-number	K802222
Device name	ANTERIOR KYPHOSIS DISTRACTION DEVICE
Applicant	Zimmer, Inc.
Product code	KWQ
Device class	Class II
Decision date	Oct 10, 1980
Decision	Substantially Equivalent
Regulation	888.3060

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View the full FDA submission: accessdata.fda.gov

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ANTERIOR KYPHOSIS DISTRACTION DEVICE

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