FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
FLEXFUSION (TM) FIXATION IMPLANT
K Number: K110445
·
Decision Mar 17, 2011
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
2
Review Days
29
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Basic Information
- Device Name
- FLEXFUSION (TM) FIXATION IMPLANT
- K Number
- K110445
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3040
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Nextremity Solutions, LLC
- Date Received
- February 16, 2011
- Decision Date
- March 17, 2011
- 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 Nextremity Solutions, LLC
| K Number | Device Name | ||
|---|---|---|---|
| K122031 | NEXTRA TI HAMMERTOE CORRECTION SYSTEM | Oct 9, 2012 | Substantially Equivalent |