The following data is part of a premarket notification filed by Ethicon Endo-surgery, Llc with the FDA for Echelon 60 Endoscpic Linear Cutter Reload, White.
| Device ID | K121600 |
| 510k Number | K121600 |
| Device Name: | ECHELON 60 ENDOSCPIC LINEAR CUTTER RELOAD, WHITE |
| Classification | Staple, Implantable |
| Applicant | ETHICON ENDO-SURGERY, LLC 4545 CREEK ROAD Cincinnati, OH 45242 |
| Contact | Asifa Vonhof |
| Correspondent | Asifa Vonhof ETHICON ENDO-SURGERY, LLC 4545 CREEK ROAD Cincinnati, OH 45242 |
| Product Code | GDW |
| CFR Regulation Number | 878.4750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-06-01 |
| Decision Date | 2012-07-16 |
| Summary: | summary |