K142887 is an FDA 510(k) clearance for the SIS Inguinal Hernia Repair Graft, a Mesh, Surgical (Class II — Special Controls, product code FTM), submitted by Cook Biotech Incorprated (West Lafayette, US). The FDA issued a Cleared decision on October 1, 2015, 364 days after receiving the submission on October 2, 2014. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.3300.
| 510(k) Number | K142887 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | October 02, 2014 |
| Decision Date | October 01, 2015 |
| Days to Decision | 364 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | FTM — Mesh, Surgical |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 878.3300 |