K153364 is an FDA 510(k) clearance for the Kerecis SecureMesh. This device is classified as a Mesh, Surgical, Collagen, Staple Line Reinforcement (Class II - Special Controls, product code OXE).
Submitted by Kerecis Limited (Isafjordur, IS). The FDA issued a Cleared decision on August 19, 2016, 273 days after receiving the submission on November 20, 2015.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.3300. For Reinforcement Of Soft Tissue Where Weakness Exists During Staple Line Reinforcement Procedures..
| 510(k) Number | K153364 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | November 20, 2015 |
| Decision Date | August 19, 2016 |
| Days to Decision | 273 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | OXE - Mesh, Surgical, Collagen, Staple Line Reinforcement |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 878.3300 |
| Definition | For Reinforcement Of Soft Tissue Where Weakness Exists During Staple Line Reinforcement Procedures. |