K-number	K101126
Device name	PONTIS SUTURES AND SUTURE ANCHORS WITH OPTIONAL CRIMPS
Applicant	Core Essence Orthopaedics, Inc.
Product code	MBI
Device class	Class II
Decision date	Dec 2, 2010
Decision	Substantially Equivalent
Regulation	888.3040

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Source

View the full FDA submission: accessdata.fda.gov

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PONTIS SUTURES AND SUTURE ANCHORS WITH OPTIONAL CRIMPS

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