FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Vail ALIF Buttress Plate System
K Number: K180755
·
Decision Jul 6, 2018
Classifications
1
FEI Numbers
356
Registration Numbers
356
Same Product Code
665
Applicant Total
5
Review Days
106
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Basic Information
- Device Name
- Vail ALIF Buttress Plate System
- K Number
- K180755
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3060
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Evolution Spine, LLC
- Date Received
- March 22, 2018
- Decision Date
- July 6, 2018
- 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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Other Clearances by Evolution Spine, LLC
| K Number | Device Name | ||
|---|---|---|---|
| K182478 | Whistler Modular Pedicle Screw System | Jan 15, 2019 | Substantially Equivalent |
| K173375 | Anterior Cervical Plate System | Dec 21, 2017 | Substantially Equivalent |
| K160663 | Lumbar Interbody Fusion System (ALIF, PLIF, LLIF, TPLIF) | Nov 16, 2016 | Substantially Equivalent |
| K160324 | Cervical Interbody Fusion System | May 5, 2016 | Substantially Equivalent |