FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MODIFICATION TO SUMMIT OCCIPITO-CERVICO-THORACIC (OCT) SPINAL SYSTEM
K Number: K022190
·
Decision Jul 24, 2002
Classifications
1
FEI Numbers
342
Registration Numbers
342
Same Product Code
302
Applicant Total
48
Review Days
19
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Basic Information
- Device Name
- MODIFICATION TO SUMMIT OCCIPITO-CERVICO-THORACIC (OCT) SPINAL SYSTEM
- K Number
- K022190
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 888.3070
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Depuyacromed
- Date Received
- July 5, 2002
- Decision Date
- July 24, 2002
- 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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| K030249 | SURGICAL TITANIUM MESH SYSTEM | Feb 14, 2003 | Substantially Equivalent |
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| K023835 | DEVEX MESH SYSTEM | Jan 29, 2003 | Substantially Equivalent |
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| K021039 | BOWTI ANTERIOR BUTTRESS STAPLE SYSTEM | Dec 11, 2002 | Substantially Equivalent |