PMA P950002S008
- Device
- BAK/L INTERBODY FUSION SYSTEM
- Applicant
- Zimmer Spine, Inc.
- PMA number
- P950002
- Supplement
- S008
- Product code
- MAX
- Decision date
- 1999-12-20
- Generic name
- Intervertebral fusion device with bone graft, lumbar
- Approval order statement
- Approval for the additional sizes to the BAK product line.
Current openFDA PMA Record#
- Device
- BAK/L INTERBODY FUSION SYSTEM
- Applicant
- Zimmer Spine, Inc.
- PMA number
- P950002
- Supplement
- S008
- Product code
- MAX
- Generic name
- Intervertebral fusion device with bone graft, lumbar
- Decision date
- 1999-12-20
- Decision code
- APPR
- Date received
- 1999-10-22
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Approval order statement
- Approval for the additional sizes to the BAK product line.