K-number	K884585
Device name	LEA PLAZA SPINAL FRAME SYSTEM
Applicant	Orthomet, Inc.
Product code	KWP
Device class	Class II
Decision date	Jan 27, 1989
Decision	Substantially Equivalent
Regulation	888.3050

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View the full FDA submission: accessdata.fda.gov

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LEA PLAZA SPINAL FRAME SYSTEM

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