K-number	K221874
Device name	Altis Single Incision Sling System
Applicant	Coloplast A/S
Product code	PAH
Device class	Class II
Decision date	Feb 15, 2023
Decision	Substantially Equivalent
Regulation	878.3300

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Source

View the full FDA submission: accessdata.fda.gov

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Altis Single Incision Sling System

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