FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
UCR SPINAL SYSTEM
K Number: K032739
·
Decision Nov 20, 2003
Classifications
1
FEI Numbers
342
Registration Numbers
342
Same Product Code
302
Applicant Total
5
Review Days
77
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Basic Information
- Device Name
- UCR SPINAL SYSTEM
- K Number
- K032739
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 888.3070
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Seaspine
- Date Received
- September 4, 2003
- Decision Date
- November 20, 2003
- Product Code
- MNI
- 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 |
|---|---|---|---|
| MNI | Orthosis, Spinal Pedicle Fixation | FDA class 2 | Orthopedic |
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Other Clearances by Seaspine
| K Number | Device Name | ||
|---|---|---|---|
| K043232 | UCR SPINAL SYSTEM | Dec 21, 2004 | Substantially Equivalent |
| K040130 | ANTERIOR LUMBAR BUTTRESS SYSTEM | Mar 26, 2004 | Substantially Equivalent |
| K032368 | SONOMA ANTERIOR CERVICAL PLATE SYSTEM | Oct 9, 2003 | Substantially Equivalent |
| K031381 | UCR SPINAL SYSTEM, LAMINAR HOOKS, PEDICLE HOOKS, AND INSTRUMENTS | Jul 30, 2003 | Substantially Equivalent |