PMA P970015S001
- Device
- NOVUS (TM) LC INTERBODY FUSION DEVICE
- Applicant
- Sofamor Danek
- PMA number
- P970015
- Supplement
- S001
- Decision date
- 1999-05-14
- Approval order statement
- Supplement received prior to original approval. This supplement was approved as part of the original approval order.
Current openFDA PMA Record#
- Device
- NOVUS (TM) LC INTERBODY FUSION DEVICE
- Applicant
- Sofamor Danek
- PMA number
- P970015
- Supplement
- S001
- Decision date
- 1999-05-14
- Decision code
- APPR
- Date received
- 1998-06-15
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- Supplement received prior to original approval. This supplement was approved as part of the original approval order.