The following data is part of a premarket notification filed by Specialty Surgical Products, Inc. with the FDA for Ventral Wall Defect Reduction Silo.
| Device ID | K973082 |
| 510k Number | K973082 |
| Device Name: | VENTRAL WALL DEFECT REDUCTION SILO |
| Classification | Mesh, Surgical, Polymeric |
| Applicant | SPECIALTY SURGICAL PRODUCTS, INC. 302 NORTH FIRST ST. Hamilton, MT 59840 |
| Contact | T. Jan Varner |
| Correspondent | T. Jan Varner SPECIALTY SURGICAL PRODUCTS, INC. 302 NORTH FIRST ST. Hamilton, MT 59840 |
| Product Code | FTL |
| CFR Regulation Number | 878.3300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-08-18 |
| Decision Date | 1997-11-04 |