FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Tri-staple 2.0 Reloads; Endo GIA Reloads with Tri-Staple Technology; Endo GIA Gray Articulating Reloads; Signia Small Diameter Reloads
K Number: K253657
·
Decision Apr 10, 2026
Classifications
1
FEI Numbers
136
Registration Numbers
136
Same Product Code
282
Applicant Total
2
Review Days
141
Basic Information
- Device Name
- Tri-staple 2.0 Reloads; Endo GIA Reloads with Tri-Staple Technology; Endo GIA Gray Articulating Reloads; Signia Small Diameter Reloads
- K Number
- K253657
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.4750
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Covidien (Part of Medtronic)
- Date Received
- November 20, 2025
- Decision Date
- April 10, 2026
- Product Code
- GDW
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- SU
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| GDW | Staple, Implantable | FDA class 2 | General, Plastic Surgery |
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FDA 510(k)
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Other Clearances by Covidien (Part of Medtronic)
| K Number | Device Name | ||
|---|---|---|---|
| K240881 | Signia Circular Adapter (Standard Length) (SIGCIRSTND); Signia Circular Adapter XL Length (SIGCIRXL) | Nov 1, 2024 | Substantially Equivalent |