PMA P950019S012
- Device
- RAY TFC DEVICE/RAY TFC UNITE DEVICE
- Applicant
- Stryker Spine
- PMA number
- P950019
- Supplement
- S012
- Product code
- MAX
- Decision date
- 2002-04-02
- Classification
- Intervertebral Fusion Device With Bone Graft, Lumbar
- Generic name
- Intervertebral fusion device with bone graft, lumbar
- Approval order statement
- APPROVAL FOR ADDITIONAL INSTRUMENTS FOR THE ALIF-OPEN SURGICAL TECHNIQUE FOR THE RAY TFC AND RAY TFC UNITE DEVICES AND REVISED LABELING.
Current openFDA PMA Record#
- Device
- RAY TFC DEVICE/RAY TFC UNITE DEVICE
- Applicant
- Stryker Spine
- PMA number
- P950019
- Supplement
- S012
- Product code
- MAX
- Generic name
- Intervertebral fusion device with bone graft, lumbar
- Decision date
- 2002-04-02
- Decision code
- APPR
- Date received
- 2002-02-11
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Approval order statement
- APPROVAL FOR ADDITIONAL INSTRUMENTS FOR THE ALIF-OPEN SURGICAL TECHNIQUE FOR THE RAY TFC AND RAY TFC UNITE DEVICES AND REVISED LABELING.