Nylamid Suture
FDA 510(k) K931612 · S. Jackson, Inc.
510(k) numberK931612
Submission
- Device name
- Nylamid Suture
- Applicant
- S. Jackson, Inc.
Alexandria, VA, US - Received
- April 1, 1993
- Decision date
- December 17, 1993
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- GAR – Suture, Nonabsorbable, Synthetic, Polyamide
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 878.5020
- Specialty
- General, Plastic Surgery
- Implant
- Yes
Other 510(k)s with product code GAR
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K261484 | Tissue Approximation SystemGAR · Special | Tas Medical, Inc. | 06/03/2026SE |
| K220980 | Tissue Approximation System (TAS)GAR · Traditional | Tas Medical, Inc. | 07/05/2023SE |
| K212888 | Golnit Nylon Monofilament SutureGAR · Abbreviated | Antarma, LLC Dba Golnit Sutures | 03/31/2022SE |
| K212603 | Non Absorbable Surgical Nylon SutureGAR · Traditional | Shandong Haidike Medical Product Co., Ltd. | 12/22/2021SE |
| K192420 | Crownjun Nylon SutureGAR · Traditional | Kono Seisakusho Co., Ltd. | 05/29/2020SE |
| K161633 | Rexlon, RexsilGAR · Traditional | Sm Eng Co., Ltd. | 03/02/2017SE |
| K151165 | Aesculap Dafilon Nonabsorbable Polyamide Surgical SutureGAR · Traditional | Aesculap, Inc. | 02/17/2016SE |
| K152795 | RiverLon (Nylon) SutureGAR · Special | Riverpoint Medical | 10/28/2015SE |
| K123034 | Vital Sutures Suturex Cirugia Peruana SutumedGAR · Traditional | Unilene Sac | 05/28/2013SE |
| K081366 | Kumar T-Anchors Hernia SetGAR · Traditional | Nashville Surgical Instruments | 07/15/2008SE |
More from Nashville Surgical Instruments
| 510(k) | Device | Decision |
|---|---|---|
| K080216 | Supramesh ExtraFTL · Traditional | 09/15/2008SE |
| K973379 | Sterile Suprafoil Smooth Nylon Foil SheetsFTM · Traditional | 09/25/1997SE |
| K931614 | Mopylen SutureGAW · Traditional | 12/17/1993SE |
| K931613 | Supramid SutureGAR · Traditional | 12/17/1993SE |
| K922630 | MopylenGAW · Traditional | 10/20/1992SE |
| K912429 | N80-838 Supramid Extra SutureGAR · Traditional | 10/02/1991SE |
| K904052 | Supramid Extra SuturesGAR · Traditional | 10/25/1990SE |
| K852011 | Nylamid Mesh Pad Full & HalfFTM · Traditional | 06/11/1985SE |
| K831725 | Foil in 3 Forms-Non-Sterile SheetsFTM · Traditional | 08/16/1983SE |
| K831727 | Quarter Globe CapsFTM · Traditional | 08/12/1983SE |
Questions and answers
When was Nylamid Suture cleared by the FDA?
Nylamid Suture (K931612) received a 510(k) decision of Substantially Equivalent on December 17, 1993, 260 days after the submission was received.
What is the product code of K931612?
The FDA product code is GAR – Suture, Nonabsorbable, Synthetic, Polyamide, a Class II (moderate risk) device regulated under 21 CFR 878.5020.