FDA 510(k)
FDA class 2
Substantially Equivalent
🇰🇷 South Korea
CastleLoc Spinal Fixation System
K Number: K162801
·
Decision Nov 3, 2016
Classifications
1
FEI Numbers
338
Registration Numbers
338
Same Product Code
308
Applicant Total
2
Review Days
29
Basic Information
- Device Name
- CastleLoc Spinal Fixation System
- K Number
- K162801
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 888.3070
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- L&K BIOMED CO., LTD.
- Date Received
- October 5, 2016
- Decision Date
- November 3, 2016
- Product Code
- MNH
- 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 |
|---|---|---|---|
| MNH | Orthosis, Spondylolisthesis Spinal Fixation | FDA class 2 | Orthopedic |
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Other Clearances by L&K BIOMED CO., LTD.
| K Number | Device Name | ||
|---|---|---|---|
| K153439 | PathLoc-C Posterior Cervical Fixation System | Jul 21, 2016 | Substantially Equivalent |