Medical Device Recalls
-
|
1 to 4 of 4 Results
510(K) Number: K180906 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Conformis iTotal Cruciate Retaining (CR) Knee Replacement System- Orthopedic Implant Cat: TCR-121-1... | 2 | 08/22/2020 |
FEI # 3009844603 Conformis, Inc. |
| iTotal CR Knee Replacement System, Model No. TCR-121-1111-010102, (ITOTAL CR IPOLY XE IMPLANT KIT LE... | 2 | 04/01/2020 |
FEI # 3009844603 Conformis, Inc. |
| iTotal CR Knee Replacement System Model Number: TCR-111-1111-010102 - Product Usage: The iTotal CR ... | 2 | 12/12/2019 |
FEI # 3009844603 Conformis, Inc. |
| iTotal CR Total Knee Replacement System, TCR-121-1111 (Catalog No.) / TCR-121-1111-010102 (Model No.... | 2 | 04/08/2019 |
FEI # 3009844603 Conformis, Inc. |
-







