The following data is part of a premarket notification filed by Vector Medical, Inc. with the FDA for Vector Targeting System.
| Device ID | K001938 |
| 510k Number | K001938 |
| Device Name: | VECTOR TARGETING SYSTEM |
| Classification | Rod, Fixation, Intramedullary And Accessories |
| Applicant | VECTOR MEDICAL, INC. 1886 LODGEPOLE DR. Milton, FL 32583 |
| Contact | Erin Mcgurk |
| Correspondent | Erin Mcgurk VECTOR MEDICAL, INC. 1886 LODGEPOLE DR. Milton, FL 32583 |
| Product Code | HSB |
| CFR Regulation Number | 888.3020 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-06-26 |
| Decision Date | 2000-08-29 |