| Device |
bone marrow processing device for clinical use |
| Definition |
Preparation of concentrated bone marrow aspirate (cBMA) from a sample of bone marrow for clinical use |
| Physical State |
May include centrifuge, filters, tubes, syringes, needles, other disposables and anticoagulant |
| Technical Method |
Uses centifugal and/or filtration methods to separate the bone marrow into components, after which the concentrated bone marrow cells are withdrawn |
| Target Area |
Bone marrow drawn from iliac crest or other bone marrow cavity, cBMA applied clinically |
| Review Panel |
Hematology |
| Product Code | PZU |
| Premarket Review |
Center for Biologics Evaluation & Research (CBER)
|
|
Not Classified Reason
|
For Export Only
|
| Submission Type |
Contact ODE
|
| Device Class |
Not Classified
|
| Total Product Life Cycle (TPLC) |
TPLC Product Code Report
|
| GMP Exempt? |
No
|
Summary Malfunction Reporting |
Ineligible |
| Implanted Device? |
No
|
| Life-Sustain/Support Device? |
No
|
| Third Party Review |
Not Third Party Eligible |