Company ยท US
Accelerated Innovation, LLC
FDA 510(k) clearances and medical device recalls filed under this name, 2008 to 2008. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| JDI | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented | 1 |
| JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 1 |
| KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 1 |
| KWQ | Appliance, Fixation, Spinal Intervertebral Body | 1 |
| KWY | Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented | 1 |
| LPH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented | 1 |
| MNH | Orthosis, Spondylolisthesis Spinal Fixation | 1 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Oct 17, 2008 | K081127 | ACCIN TOTAL KNEE SYSTEM Accelerated Innovation, LLC | JWH |
| Jul 8, 2008 | K080647 | ACCIN BIPOLAR HEAD SYSTEM Accelerated Innovation, LLC | KWY |
| Jun 2, 2008 | K080539 | ACCIN UNIPOLAR HEAD SYSTEM Accelerated Innovation, LLC | JDI |
| Feb 29, 2008 | K073120 | ACCIN PATELLOFEMORAL SYSTEM Accelerated Innovation, LLC | KRR |
| Feb 4, 2008 | K073531 | ACCIN PEDICLE SCREW SYSTEM Accelerated Innovation, LLC | MNH |
| Jan 31, 2008 | K073530 | ACCIN ANTERIOR CERVICAL PLATE SYSTEM Accelerated Innovation, LLC | KWQ |
| Jan 10, 2008 | K073068 | ACCIN HIP SYSTEM Accelerated Innovation, LLC | LPH |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||