Premium
FDA 510(k) K133889 · Cousin Biotech Sas
510(k) numberK133889
Submission
- Device name
- Premium
- Applicant
- Cousin Biotech Sas
Wervicq-Sud, FR - Received
- December 20, 2013
- Decision date
- September 4, 2014
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- FTL – Mesh, Surgical, Polymeric
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 878.3300
- Specialty
- General, Plastic Surgery
- Implant
- Yes
Other 510(k)s with product code FTL
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K253956 | ProGrip advanced self-gripping polypropylene mesh (ADG1510, ADG2015, ADG3020, ADG4030)FTL · Traditional | Sofradim Production | 05/21/2026SE |
| K253125 | Parietene Flat Sheet MeshFTL · Special | Medtronic - Sofradim Production | 10/24/2025SE |
| K251955 | Onflex MeshFTL · Special | Davol Inc., Subsidiary of C. R. Bard, Inc. | 07/24/2025SE |
| K251557 | Bard® Mesh; Bard® Mesh Pre-ShapedFTL · Special | Davol, Inc. | 06/12/2025SE |
| K250869 | Parietene Macroporous Mesh (PPM5050 )FTL · Special | Sofradim Production | 04/23/2025SE |
| K250098 | Bard Soft Mesh; Bard Soft Mesh Pre-ShapedFTL · Traditional | Davol, Inc. | 04/09/2025SE |
| K243315 | ProGrip Self-Gripping Polypropylene MeshFTL · Traditional | Sofradim Production | 01/17/2025SE |
| K241250 | 3DMax Light MeshFTL · Special | Davol Inc., Subsidiary of C. R. Bard, Inc. | 06/14/2024SE |
| K232373 | Progrip Self-Gripping Polypropylene MeshFTL · Traditional | Sofradim Production | 01/18/2024SE |
| K233402 | Bard 3DMax MeshFTL · Special | Davol Inc., Subsidiary of C. R. Bard, Inc. | 11/01/2023SE |
More from Davol Inc., Subsidiary of C. R. Bard, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K181086 | Cortical Fixation SystemsMBI · Traditional | 01/09/2019SE |
| K181799 | ResCUBE Ligament Fixation SystemOWI · Traditional | 08/29/2018SE |
| K172206 | NAJA Ligament Correction SystemOWI · Traditional | 04/10/2018SE |
| K093196 | Biomesh Ca.B.S. 'Air Composite, Models: CABST1R05T, CABSAIRC7, CABSAIRC09FTL · Abbreviated | 06/25/2010SE |
| K072962 | Cabs'AirFTL · Traditional | 06/26/2008SE |
| K070918 | 4DDOMEFTL · Traditional | 08/22/2007SE |
Questions and answers
When was Premium cleared by the FDA?
Premium (K133889) received a 510(k) decision of Substantially Equivalent on September 4, 2014, 258 days after the submission was received.
What is the product code of K133889?
The FDA product code is FTL – Mesh, Surgical, Polymeric, a Class II (moderate risk) device regulated under 21 CFR 878.3300.