Coloplast Corp. · Class II · Cleared Oct 18, 2024
| K-number | K242473 |
| Device name | Altis Single Incision Sling System (519650); Aris Transobturator Sling System (519551); Supris Retropubic Sling System (519562) |
| Applicant | Coloplast Corp. |
| Product code | PAH |
| Device class | Class II |
| Decision date | Oct 18, 2024 |
| Decision | Substantially Equivalent |
| Regulation | 878.3300 |
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