RAY TFC DEVICE WITH INSTRUMENTATION (20MM)
FDA premarket approval P950019/S003 · decided 1998-06-17
Approval details
- PMA number
- P950019
- Supplement
- S003
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- RAY TFC DEVICE WITH INSTRUMENTATION (20MM)
- Generic name
- Intervertebral fusion device with bone graft, lumbar
- Applicant
- Stryker Spine
- Date received
- 1998-05-15
- Decision date
- 1998-06-17
- Days to decision
- 33 days
- Decision code
- APPR
- Product code
- MAX
- Advisory committee
- Orthopedic
- Expedited review
- No
- Location
- Allendale, NJ
- Statement
- Approval for the addition of 20mm cages and modified labeling.
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