FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Synchfix EVT
K Number: K251643
·
Decision Oct 29, 2025
Classifications
1
FEI Numbers
272
Registration Numbers
272
Same Product Code
92
Applicant Total
2
Review Days
153
Basic Information
- Device Name
- Synchfix EVT
- K Number
- K251643
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3030
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Wright Medical Technology, Inc. (Stryker Corporation)
- Date Received
- May 29, 2025
- Decision Date
- October 29, 2025
- Product Code
- HTN
- 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 |
|---|---|---|---|
| HTN | Washer, Bolt Nut | FDA class 2 | Orthopedic |
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Other Clearances by Wright Medical Technology, Inc. (Stryker Corporation)
| K Number | Device Name | ||
|---|---|---|---|
| K252085 | Allomatrix (Allomatrix Injectable Putty; Allomatrix C; Allomatrix DR; Allomatrix Custom) | Sep 30, 2025 | Substantially Equivalent |