FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Stimulator, Bone Growth, Non-Invasive
PMA: P910066
·
Supplement: S022
·
Decision Oct 13, 2006
Classifications
1
FEI Numbers
17
Registration Numbers
17
Basic Information
- Device Name
- Stimulator, Bone Growth, Non-Invasive
- Trade Name
- OL1000/OL1000 SC AND SPINALOGIC BONE GROWTH STIMULATOR
- PMA Number
- P910066
- Supplement Number
- S022
- 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
- October 13, 2006
- Date Received
- August 31, 2006
- Supplement Type
- Normal 180 Day Track No User Fee
- Supplement Reason
- Express GMP Supplement
- Expedited Review
- N
Advisory Committee Statement
APPROVAL FOR A MANUFACTURING SITE LOCATED IN VISTA, CALIFORNIA.
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 |