FDA 510(k)
FDA class 2
Substantially Equivalent
🇧🇷 Brazil
Cannulated Screws Neoortho
K Number: K162874
·
Decision Jun 27, 2017
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
5
Review Days
257
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Basic Information
- Device Name
- Cannulated Screws Neoortho
- K Number
- K162874
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3040
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Neoortho Produtos Ortopedicos S/A
- Date Received
- October 13, 2016
- Decision Date
- June 27, 2017
- Product Code
- HWC
- Advisory Committee
- Orthopedic
- Review Advisory Committee
- OR
- 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 |
|---|---|---|---|
| HWC | Screw, Fixation, Bone | FDA class 2 | Orthopedic |
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Other Clearances by Neoortho Produtos Ortopedicos S/A
| K Number | Device Name | ||
|---|---|---|---|
| K141103 | INTRAMEDULLARY NAIL AND SCREWS-NEONAIL | Sep 23, 2014 | Substantially Equivalent |
| K132852 | PEEK CAGE FOR THE VERTEBRAL SPINE | May 29, 2014 | Substantially Equivalent |
| K113733 | SMALL AND LARGE FRAGMENTS OSTEOSYNTHESIS SYSTEM NEOFIX | Mar 23, 2012 | Substantially Equivalent |
| K102641 | MINI AND MICRO FRAGMENTS RECONSTRUCTION SYSTEM-NEOFACE | Dec 20, 2010 | Substantially Equivalent |