FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Stimulator, Bone Growth, Non-Invasive
PMA: P030034
·
Supplement: S010
·
Decision Jun 22, 2017
Classifications
1
FEI Numbers
17
Registration Numbers
17
Basic Information
- Device Name
- Stimulator, Bone Growth, Non-Invasive
- Trade Name
- CervicalStim
- PMA Number
- P030034
- Supplement Number
- S010
- Device Class
- FDA Class 3
- Product Code
- LOF
- Generic Name
- Stimulator, bone growth, non-invasive
- Medical Specialty
- Unknown
- Advisory Committee
- Orthopedic
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- June 22, 2017
- Date Received
- March 24, 2017
- Supplement Type
- Real-Time Process
- Supplement Reason
- Change Design/Components/Specifications/Material
- Expedited Review
- N
Advisory Committee Statement
Approval for software and firmware updates to the SpinalStim and CervicalStim devices. The updates made are identical to both devices, and include modifications to the user display and mobile medical phone application
Classifications
This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| LOF | Stimulator, Bone Growth, Non-Invasive | FDA class 3 | Unknown |