K-number	K073177
Device name	PIONEER INTERVERTEBRAL FUSION DEVICE SYSTEM
Applicant	Pioneer Surgical Technology
Product code	MAX
Device class	Class II
Decision date	May 13, 2008
Decision	Substantially Equivalent
Regulation	888.3080

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View the full FDA submission: accessdata.fda.gov

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PIONEER INTERVERTEBRAL FUSION DEVICE SYSTEM

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