FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Sovereign Posterior Cervical System
K Number: K250866
·
Decision May 20, 2025
Classifications
1
FEI Numbers
164
Registration Numbers
164
Same Product Code
117
Applicant Total
4
Review Days
57
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Basic Information
- Device Name
- Sovereign Posterior Cervical System
- K Number
- K250866
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3075
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Met One Technologies, LLC
- Date Received
- March 24, 2025
- Decision Date
- May 20, 2025
- Product Code
- NKG
- 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 |
|---|---|---|---|
| NKG | Posterior Cervical Screw System | FDA class 2 | Orthopedic |
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