K-number	K930156
Device name	MEGA PLUS SUPER LAG SCREW
Applicant	Pfizer Hospital Products Group, Inc.
Product code	KTT
Device class	Class II
Decision date	Feb 22, 1994
Decision	Substantially Equivalent
Regulation	888.3030

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View the full FDA submission: accessdata.fda.gov

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MEGA PLUS SUPER LAG SCREW

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