The following data is part of a premarket notification filed by W.l. Gore & Associates,inc with the FDA for Gore-tex Dualmesh Plus Biomaterial (1 Mm & 2mm).
| Device ID | K000185 |
| 510k Number | K000185 |
| Device Name: | GORE-TEX DUALMESH PLUS BIOMATERIAL (1 MM & 2MM) |
| Classification | Mesh, Surgical, Polymeric |
| Applicant | W.L. GORE & ASSOCIATES,INC 3450 WEST KILTIE LN. Flagstaff, AZ 86002 -0500 |
| Contact | R. Larry Pratt |
| Correspondent | R. Larry Pratt W.L. GORE & ASSOCIATES,INC 3450 WEST KILTIE LN. Flagstaff, AZ 86002 -0500 |
| Product Code | FTL |
| CFR Regulation Number | 878.3300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-01-20 |
| Decision Date | 2000-02-14 |