FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Camber Sacroiliac (SI) Fixation System
K Number: K203503
·
Decision Sep 2, 2022
Classifications
1
FEI Numbers
155
Registration Numbers
155
Same Product Code
130
Applicant Total
6
Review Days
641
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Basic Information
- Device Name
- Camber Sacroiliac (SI) Fixation System
- K Number
- K203503
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3040
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Camber Spine Technologies, LLC
- Date Received
- November 30, 2020
- Decision Date
- September 2, 2022
- Product Code
- OUR
- 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 |
|---|---|---|---|
| OUR | Sacroiliac Joint Fixation | FDA class 2 | Orthopedic |
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Other Clearances by Camber Spine Technologies, LLC
| K Number | Device Name | ||
|---|---|---|---|
| K232256 | Alcantara Thoracolumbar Plate System | Apr 16, 2024 | Substantially Equivalent |
| K210595 | SPIRA-T Oblique Posterior Lumbar Spacers, SPIRA-P Posterior Lumbar Spacers | Jun 15, 2021 | Substantially Equivalent |
| K191584 | FORTICO Anterior Cervical Fixation System | Oct 22, 2019 | Substantially Equivalent |
| K180980 | ORTHROS Posterior Stabilization System; ORTHROS MIS Posterior Stabilization System | Oct 27, 2018 | Substantially Equivalent |
| K180724 | SPIRA Open Matrix LLIF | Jun 25, 2018 | Substantially Equivalent |