Endotine Ribbon
FDA 510(k) K051415 · Coapt Systems, Inc.
510(k) numberK051415
Submission
- Device name
- Endotine Ribbon
- Applicant
- Coapt Systems, Inc.
Palo Alto, CA, US - Received
- June 1, 2005
- Decision date
- June 23, 2005
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- GAM – Suture, Absorbable, Synthetic, Polyglycolic Acid
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 878.4493
- Specialty
- General, Plastic Surgery
- Implant
- Yes
Other 510(k)s with product code GAM
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K253394 | Coated VICRYL (Polyglactin 910) Plus Antibacterial SutureGAM · Traditional | ETHICON, Inc. | 06/25/2026SE |
| K253530 | Trexon Monofilament Synthetic Absorbable SutureGAM · Traditional | Medtronic | 05/28/2026SE |
| K253852 | MONOCRYL Plus Antibacterial Poliglecaprone 25 (Monofilament), Sterile Synthetic…GAM · Traditional | ETHICON, Inc. | 02/06/2026SE |
| K252743 | STRATAFIX Spiral PDS Plus Knotless Tissue Control Device; STRATAFIX Spiral MONOCRYL…GAM · Traditional | ETHICON, Inc. | 12/22/2025SE |
| K253620 | TroClose 1200GAM · Special | Gordian Surgical, Ltd. | 12/16/2025SE |
| K252820 | PGLA90 Poly(glycolide-co-L-lactide) Surgical Sutures (Calypso); PGLA90…GAM · Special | Internacional Farmacéutica S.A DE C.V | 10/03/2025SE |
| K233265 | Monotime and Optime RGAM · Abbreviated | Peters Surgical | 10/11/2024SE |
| K232372 | Peters Surgical ADVANTIME Absorbable Suture (ADVANTIME)GAM · Abbreviated | Peters Surgical | 07/12/2024SE |
| K221527 | StitchKitGAM · Traditional | Origami Surgical Inc . | 02/14/2023SE |
| K221744 | STRATAFIX Spiral MONOCRYL Plus Knotless Tissue Control DeviceGAM · Traditional | ETHICON, Inc. | 11/15/2022SE |
More from ETHICON, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K083783 | VF LiquigelMIX · Traditional | 09/11/2009SE |
| K080956 | Modification to VF Gel PlusMIX · Special | 04/25/2008SE |
| K071663 | VF Gel PlusMIX · Traditional | 02/15/2008SE |
| K060249 | Ultratine ForeheadHWC · Traditional | 06/12/2006SE |
| K060248 | Ultratine TransblephHWC · Traditional | 06/12/2006SE |
| K060828 | Modification to Endotine RibbonGAM · Special | 04/19/2006SE |
| K050611 | Endotine RibbonGAM · Special | 04/06/2005SE |
| K042796 | Endotine Transbleph 3.0/3.5 DeviceHWC · Special | 11/05/2004SE |
| K041835 | Endotine Midface B 4.5 DeviceHWC · Traditional | 09/28/2004SE |
| K042078 | Endotine Forehead Triple DeviceHWC · Special | 08/27/2004SE |
Questions and answers
When was Endotine Ribbon cleared by the FDA?
Endotine Ribbon (K051415) received a 510(k) decision of Substantially Equivalent on June 23, 2005, 22 days after the submission was received.
What is the product code of K051415?
The FDA product code is GAM – Suture, Absorbable, Synthetic, Polyglycolic Acid, a Class II (moderate risk) device regulated under 21 CFR 878.4493.