K153307 is an FDA 510(k) clearance for the HS SutureTape, a Suture, Nonabsorbable, Synthetic, Polyethylene (Class II — Special Controls, product code GAT), submitted by Riverpoint Medical (Portland, US). The FDA issued a Cleared decision on February 12, 2016, 88 days after receiving the submission on November 16, 2015. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.5000.
| 510(k) Number | K153307 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | November 16, 2015 |
| Decision Date | February 12, 2016 |
| Days to Decision | 88 days |
| Submission Type | Special |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | GAT — Suture, Nonabsorbable, Synthetic, Polyethylene |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 878.5000 |