K-number	K093719
Device name	PRO-FIX PRECISION FIXATION SYSTEM MODEL PFM#, PFB#, PFT#
Applicant	Osteogenics Biomedical, Inc.
Product code	DZL
Device class	Class II
Decision date	Mar 1, 2010
Decision	Substantially Equivalent
Regulation	872.4880

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View the full FDA submission: accessdata.fda.gov

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PRO-FIX PRECISION FIXATION SYSTEM MODEL PFM#, PFB#, PFT#

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