| Primary Device ID | B0462201020050 | 
| NIH Device Record Key | 26c15c8d-5139-409c-817e-36bc36aaee1a | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Symmetric TK Femoral Component | 
| Version Model Number | 5LT | 
| Catalog Number | 22-01-02005 | 
| Company DUNS | 169289308 | 
| Company Name | SIGNAL MEDICAL CORPORATION | 
| Device Count | 1 | 
| DM Exempt | false | 
| Pre-market Exempt | false | 
| MRI Safety Status | Labeling does not contain MRI Safety Information | 
| Human Cell/Tissue Product | false | 
| Device Kit | false | 
| Device Combination Product | false | 
| Single Use | true | 
| Lot Batch | true | 
| Serial Number | true | 
| Manufacturing Date | true | 
| Expiration Date | true | 
| Donation Id Number | false | 
| Contains Natural Rubber Latex | false | 
| Labeled No Natural Rubber Latex | false | 
| RX Perscription | true | 
| OTC Over-The-Counter | false | 
| Phone | 810-364-7070 | 
| jgorney@signalmd.com | |
| Phone | 810-364-7070 | 
| jgorney@signalmd.com | 
| Device Issuing Agency | Device ID | 
|---|---|
| HIBCC | B0462201020050 [Primary] | 
| JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 
| Steralize Prior To Use | false | 
| Device Is Sterile | true | 
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 3 | 
| Public Version Date | 2018-07-06 | 
| Device Publish Date | 2016-02-12 | 
| B046220102104 | 4RT Symmetric TK Femoral Component | 
| B0462201021050 | 5RT Symmetric TK Femoral Component | 
| B0462201020070 | 7LT Symmetric TK Femoral Component | 
| B0462201020060 | Symmetric TK Femoral Component 6LT | 
| B0462201020050 | 5LT Symmetric TK Femoral Component | 
| B0462201020040 | 4LT Symmetric TK Femoral Component | 
| B0462201021030 | 3RT Symmetric TK Femoral Component | 
| B0462201020030 | 3LT Symmetric TK Femoral Component |