Class Class II

Altis Single Incision Sling System (K221874)

K221874 2023-02-15 Special
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Description

Altis Single Incision Sling System by Coloplast A/S — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK221874
Clearance Date2023-02-15
Clearance TypeSpecial
Product CodePAH
Regulation Number878.3300

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