The following data is part of a premarket notification filed by Biodynamic Technologies, Inc. with the FDA for Fx-cablelok System, Modification.
| Device ID | K915259 |
| 510k Number | K915259 |
| Device Name: | FX-CABLELOK SYSTEM, MODIFICATION |
| Classification | Cerclage, Fixation |
| Applicant | BIODYNAMIC TECHNOLOGIES, INC. 727 TWENTY-THIRD ST. SOUTH Arlington, VA 22202 |
| Contact | Andrew E Taylor |
| Correspondent | Andrew E Taylor BIODYNAMIC TECHNOLOGIES, INC. 727 TWENTY-THIRD ST. SOUTH Arlington, VA 22202 |
| Product Code | JDQ |
| CFR Regulation Number | 888.3010 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-11-19 |
| Decision Date | 1992-02-07 |