FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DeGen Navigated Instrumentation
K Number: K213918
·
Decision Feb 9, 2022
Classifications
1
FEI Numbers
381
Registration Numbers
381
Same Product Code
430
Applicant Total
16
Review Days
56
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Basic Information
- Device Name
- DeGen Navigated Instrumentation
- K Number
- K213918
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.4560
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Degen Medical
- Date Received
- December 15, 2021
- Decision Date
- February 9, 2022
- Product Code
- OLO
- Advisory Committee
- Neurology
- 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 |
|---|---|---|---|
| OLO | Orthopedic Stereotaxic Instrument | FDA class 2 | Neurology |
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| K241077 | DeGen Medical Patient Specific Implant (PSI) System | Oct 29, 2024 | Substantially Equivalent |
| K231199 | Solar Lumbar Interbody Fusion System | Jun 16, 2023 | Substantially Equivalent |
| K223418 | DeGen Impulse AM System | Mar 17, 2023 | Substantially Equivalent |
| K213901 | Cyclops Anterior Cervical Plate System | Jan 7, 2022 | Substantially Equivalent |
| K210090 | Impulse AM Interbody Fusion System | Aug 30, 2021 | Substantially Equivalent |
| K203816 | DeGen Navigated Instrumentation | Apr 2, 2021 | Substantially Equivalent |
| K201287 | Impulse Interbody Fusion System | Dec 22, 2020 | Substantially Equivalent |