FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SOVEREIGN SPINAL SYSTEM
K Number: K110063
·
Decision Oct 4, 2011
Classifications
1
FEI Numbers
253
Registration Numbers
253
Same Product Code
200
Applicant Total
99
Review Days
267
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Basic Information
- Device Name
- SOVEREIGN SPINAL SYSTEM
- K Number
- K110063
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3080
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Medtronic Sofamor Danek, Inc.
- Date Received
- January 10, 2011
- Decision Date
- October 4, 2011
- Product Code
- OVD
- 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 |
|---|---|---|---|
| OVD | Intervertebral Fusion Device With Integrated Fixation, Lumbar | FDA class 2 | Orthopedic |
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|---|---|---|---|
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| K243706 | Mastergraft Matrix EXT; Mastergraft Strip; Mastergraft Putty; Mastergraft Granules | Jan 17, 2025 | Substantially Equivalent |
| K230716 | Robotic Graft Delivery Instruments | Jul 18, 2023 | Substantially Equivalent |
| K141824 | MASTERGRAFT MATRIX EXT; MASTERGRAFT PUTTY, MASTERGRAFT STRIP | Sep 5, 2014 | Substantially Equivalent |
| K140417 | DIVERGENCE MINI-PLATE ANTERIOR CERVICAL FUSION SYSTEM | Jul 9, 2014 | Substantially Equivalent |
| K140449 | CD HORIZON SPINAL SYSTEM | Mar 25, 2014 | Substantially Equivalent |
| K132897 | CLYDESDALE SPINAL SYSTEM | Dec 11, 2013 | Substantially Equivalent |
| K133216 | CRESCENT SPINAL SYSTEM | Nov 22, 2013 | Substantially Equivalent |
| K132700 | PERIMETER INTERBODY FUSION DEVICE | Sep 26, 2013 | Substantially Equivalent |
| K131888 | T2 XVBR SPINAL SYSTEM, T2 ALTITUDE EXPANDABLE CORPECTOMY DEVICE | Sep 23, 2013 | Substantially Equivalent |