FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
KAPSS SPINAL SYSTEM
K Number: K093833
·
Decision Oct 15, 2010
Classifications
1
FEI Numbers
342
Registration Numbers
342
Same Product Code
302
Applicant Total
2
Review Days
305
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Basic Information
- Device Name
- KAPSS SPINAL SYSTEM
- K Number
- K093833
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3070
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Robert Reid, Inc.
- Date Received
- December 14, 2009
- Decision Date
- October 15, 2010
- 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 Robert Reid, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K093089 | MAGNUM NAIL | Nov 13, 2009 | Substantially Equivalent |