K-number	K070130
Device name	ORBITAL RECONSTRUCTIVE IMPLANT
Applicant	Becker & Associates Consulting, Inc.
Product code	HPZ
Device class	Class II
Decision date	Apr 19, 2007
Decision	Substantially Equivalent
Regulation	886.3320

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Source

View the full FDA submission: accessdata.fda.gov

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ORBITAL RECONSTRUCTIVE IMPLANT

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