The following data is part of a premarket notification filed by Sofamor Co. with the FDA for Rod For Rachis Surgery.
| Device ID | K843687 |
| 510k Number | K843687 |
| Device Name: | ROD FOR RACHIS SURGERY |
| Classification | Appliance, Fixation, Spinal Interlaminal |
| Applicant | SOFAMOR CO. ONE STUART PLAZA DONOHUE/LUXOR ROADS Greensburg, PA 15601 |
| Contact | Abraham Glasser |
| Correspondent | Abraham Glasser SOFAMOR CO. ONE STUART PLAZA DONOHUE/LUXOR ROADS Greensburg, PA 15601 |
| Product Code | KWP |
| CFR Regulation Number | 888.3050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-09-18 |
| Decision Date | 1985-01-10 |