FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
T-PLATE ANTERIOR FIXATION SYSTEM
K Number: K051764
·
Decision Jul 13, 2005
Classifications
1
FEI Numbers
356
Registration Numbers
356
Same Product Code
665
Applicant Total
1
Review Days
13
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Basic Information
- Device Name
- T-PLATE ANTERIOR FIXATION SYSTEM
- K Number
- K051764
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3060
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Esm Technologies
- Date Received
- June 30, 2005
- Decision Date
- July 13, 2005
- Product Code
- KWQ
- 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 |
|---|---|---|---|
| KWQ | Appliance, Fixation, Spinal Intervertebral Body | FDA class 2 | Orthopedic |
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