The following data is part of a premarket notification filed by C.r. Bard, Inc. with the FDA for Ajust Helical Adjustable Single-incision Sling.
| Device ID | K123179 |
| 510k Number | K123179 |
| Device Name: | AJUST HELICAL ADJUSTABLE SINGLE-INCISION SLING |
| Classification | Mesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Female, Mini-sling |
| Applicant | C.R. BARD, INC. 8195 INDUSTRIAL BLVD. Covington, GA 30014 |
| Contact | Michele Davis |
| Correspondent | Michele Davis C.R. BARD, INC. 8195 INDUSTRIAL BLVD. Covington, GA 30014 |
| Product Code | PAH |
| CFR Regulation Number | 878.3300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-10-09 |
| Decision Date | 2012-11-02 |
| Summary: | summary |