FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SeaSpine Cambria System
K Number: K171046
·
Decision Jul 7, 2017
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
66
Review Days
91
Basic Information
- Device Name
- SeaSpine Cambria System
- K Number
- K171046
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3080
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- SeaSpine Orthopedics Corporation
- Date Received
- April 7, 2017
- Decision Date
- July 7, 2017
- Product Code
- ODP
- 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 |
|---|---|---|---|
| ODP | Intervertebral Fusion Device With Bone Graft, Cervical | FDA class 2 | Orthopedic |
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Other Clearances by SeaSpine Orthopedics Corporation
| K Number | Device Name | ||
|---|---|---|---|
| K250908 | Virata Spinal Fixation System | Jun 18, 2025 | Substantially Equivalent |
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| K233694 | Meridian Interbody System; WaveForm A Interbody System | Jan 12, 2024 | Substantially Equivalent |
| K233414 | Shoreline ACS Interbody System; Shoreline RT Interbody System | Nov 28, 2023 | Substantially Equivalent |
| K232668 | Cove Strip, OsteoCove Strip | Sep 27, 2023 | Substantially Equivalent |
| K231030 | Cove Putty, OsteoCove Putty | Sep 14, 2023 | Substantially Equivalent |