K170945 is an FDA 510(k) clearance for the Biodesign Staple Line Reinforcement. This device is classified as a Mesh, Surgical, Collagen, Staple Line Reinforcement (Class II - Special Controls, product code OXE).
Submitted by Cook Biotech Incorporated (West Lafayetta, US). The FDA issued a Cleared decision on April 28, 2017, 29 days after receiving the submission on March 30, 2017.
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 | K170945 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 30, 2017 |
| Decision Date | April 28, 2017 |
| Days to Decision | 29 days |
| Submission Type | Special |
| 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. |