The following data is part of a premarket notification filed by Surgitek with the FDA for Surgitek Super Double J Ureteral Stent Kit.
| Device ID | K880660 |
| 510k Number | K880660 |
| Device Name: | SURGITEK SUPER DOUBLE J URETERAL STENT KIT |
| Classification | Stent, Ureteral |
| Applicant | SURGITEK 3037 MT. PLEASANT ST. Racine, WI 53404 |
| Contact | Waxberg |
| Correspondent | Waxberg SURGITEK 3037 MT. PLEASANT ST. Racine, WI 53404 |
| Product Code | FAD |
| CFR Regulation Number | 876.4620 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-02-17 |
| Decision Date | 1988-04-14 |