K-number	K220050
Device name	KLS Martin IPS Distraction
Applicant	KLS Martin L.P.
Product code	MQN
Device class	Class II
Decision date	Aug 11, 2022
Decision	Substantially Equivalent
Regulation	872.4760

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Source

View the full FDA submission: accessdata.fda.gov

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KLS Martin IPS Distraction

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