K-number	K041425
Device name	CONSERVE PLUS REVISION SHELL AND CONSERVE PLUS THICK SHELL
Applicant	Wrightmedicaltechnologyinc
Product code	KWA
Device class	Class III
Decision date	Jun 25, 2004
Decision	Substantially Equivalent
Regulation	888.3330

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Source

View the full FDA submission: accessdata.fda.gov

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CONSERVE PLUS REVISION SHELL AND CONSERVE PLUS THICK SHELL

Everything you need for a 510(k) submission. Nothing you don't.