The following data is part of a premarket notification filed by Medical Marketing, Inc. with the FDA for Titanium Rods.
| Device ID | K874612 |
| 510k Number | K874612 |
| Device Name: | TITANIUM RODS |
| Classification | Laparoscope, Gynecologic (and Accessories) |
| Applicant | MEDICAL MARKETING, INC. P.O. BOX 222 Fischer, TX 78623 |
| Contact | Dan E Edwards |
| Correspondent | Dan E Edwards MEDICAL MARKETING, INC. P.O. BOX 222 Fischer, TX 78623 |
| Product Code | HET |
| CFR Regulation Number | 884.1720 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-11-09 |
| Decision Date | 1988-06-23 |