ECHELON FLEX POWERED PLUS ARTICULATING ENDOSCOPIC LINEAR CUTTER, 60MM, STANDARD, ECHELON FLEX POWERED PLUS ARTICULATING— 510(k) K140560
Substantially EquivalentEthicon Endo-Surgery, LLC
FDA 510(k) clearance K140560 for ECHELON FLEX POWERED PLUS ARTICULATING ENDOSCOPIC LINEAR CUTTER, 60MM, STANDARD, ECHELON FLEX POWERED PLUS ARTICULATING, Substantially Equivalent on 2014-04-22. Applicant: Ethicon Endo-Surgery, LLC. Device class: 2.
Clearance details
- Applicant
- Ethicon Endo-Surgery, LLC
- Product code
- Code GDW
- Device class
- Class 2
- Regulation
- 21 CFR 878.4750
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Cincinnati, OH, US
Recent devices under product code GDW
view allMore clearances from Ethicon Endo-Surgery, LLC
view all- K252906 — ECHELON ENDOPATH Staple Line Reinforcement (ECH60R)
- K241630 — ECHELON 4000 60mm Compact Stapler (EC3D60C) +6 more
- K241629 — ECHELON 3000 45mm Compact Stapler (ECH45C) +5 more
- K232313 — LIGACLIP Endoscopic Rotating Multiple Clip Applier 12mm L (ER420) +1 more
- K230387 — ENSEAL X1 Curved Tissue Sealers, 25 cm shaft length (NSLX125C) +4 more
Adverse events under product code GDW
product code GDW- Death
- 450
- Injury
- 12,684
- Malfunction
- 68,730
- Other
- 6
- Total
- 81,870
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Recalls naming K140560
K-number listed on FDA's recall record- Z-0202-2020 — ECHELON FLEX Powered Plus ENDOPATH 60mm Stapler - 440mm shaft, Product Code PLEE60A
- Z-0203-2020 — ECHELON FLEX Powered Plus ENDOPATH 60mm Stapler - 340mm shaft, Product Code PSEE60A
Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K140560.
Data sourced from openFDA. This site is unofficial and independent of the FDA.