FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Spinal Pedicle Screw, Fixation, Appliance System
PMA: P960025
·
Supplement: S010
·
Decision Mar 17, 2004
Classifications
1
FEI Numbers
2
Registration Numbers
2
Basic Information
- Device Name
- Spinal Pedicle Screw, Fixation, Appliance System
- Trade Name
- LUMBAR I/F CAGE SYSTEM
- PMA Number
- P960025
- Supplement Number
- S010
- Device Class
- FDA Class 3
- Product Code
- MCV
- Generic Name
- SPINAL PEDICLE SCREW, FIXATION, APPLIANCE SYSTEM
- Medical Specialty
- Unknown
- Advisory Committee
- Orthopedic
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- March 17, 2004
- Date Received
- February 24, 2003
- Supplement Type
- Normal 180 Day Track
- Supplement Reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
APPROVAL FOR A MANUFACTURING SITE LOCATED AT DEPUY ACROMED SARL, LELOCLE, SWITZERLAND.
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 |
|---|---|---|---|
| MCV | Spinal Pedicle Screw, Fixation, Appliance System | FDA class 3 | Unknown |