K-number	K863447
Device name	STRYKER ORTHOPOWER 90 & ORTHOPOWER 90 SYSTEM II
Applicant	Stryker Corp.
Product code	GET
Device class	Class I
Decision date	Sep 29, 1986
Decision	Substantially Equivalent
Regulation	878.4820

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View the full FDA submission: accessdata.fda.gov

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STRYKER ORTHOPOWER 90 & ORTHOPOWER 90 SYSTEM II

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