Kumar T-Anchors Hernia Set
FDA 510(k) K081366 · Nashville Surgical Instruments
510(k) numberK081366
Submission
- Device name
- Kumar T-Anchors Hernia Set
- Applicant
- Nashville Surgical Instruments
Springfield, TN, US - Received
- May 15, 2008
- Decision date
- July 15, 2008
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary 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 |
| K060471 | FSSB Nylon Surgical SuturesGAR · Abbreviated | Fssb Chirurgische Nadeln GmbH | 07/26/2006SE |
More from Fssb Chirurgische Nadeln GmbH
| 510(k) | Device | Decision |
|---|---|---|
| K973621 | Pre-View Cholangiography ClampGBZ · Traditional | 12/17/1997SE |
Questions and answers
When was Kumar T-Anchors Hernia Set cleared by the FDA?
Kumar T-Anchors Hernia Set (K081366) received a 510(k) decision of Substantially Equivalent on July 15, 2008, 61 days after the submission was received.
What is the product code of K081366?
The FDA product code is GAR – Suture, Nonabsorbable, Synthetic, Polyamide, a Class II (moderate risk) device regulated under 21 CFR 878.5020.