FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SPINAL ELEMENTS CERCLAGE SYSTEM
K Number: K120177
·
Decision Jul 3, 2012
Classifications
1
FEI Numbers
155
Registration Numbers
155
Same Product Code
128
Applicant Total
49
Review Days
165
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Basic Information
- Device Name
- SPINAL ELEMENTS CERCLAGE SYSTEM
- K Number
- K120177
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3010
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Spinal Elements, Inc.
- Date Received
- January 20, 2012
- Decision Date
- July 3, 2012
- Product Code
- JDQ
- 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 |
|---|---|---|---|
| JDQ | Cerclage, Fixation | FDA class 2 | Orthopedic |
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Other Clearances by Spinal Elements, Inc.
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|---|---|---|---|
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| K242527 | The Karma® Fixation System | May 21, 2025 | Substantially Equivalent |
| K243916 | Primus Spinal Fixation System | Feb 21, 2025 | Substantially Equivalent |
| K231593 | Sapphire X3 Anterior Cervical Plate System | Aug 2, 2023 | Substantially Equivalent |
| K231252 | Ventana L Spinal System | Jun 30, 2023 | Substantially Equivalent |
| K222833 | Ventana C Spinal System | May 19, 2023 | Substantially Equivalent |
| K222516 | Mercury® II Spinal System | Dec 1, 2022 | Substantially Equivalent |
| K210044 | Crystal Spinal System & Vertu Spinal System, Lucent Spinal System, Zeus Spinal System, Ceres-C Spinal System, Omega XP Spinal System | Jun 30, 2021 | Substantially Equivalent |