The following data is part of a premarket notification filed by Osteomed with the FDA for Osteomed Extremifuse System.
| Device ID | K140283 |
| 510k Number | K140283 |
| Device Name: | OSTEOMED EXTREMIFUSE SYSTEM |
| Classification | Screw, Fixation, Bone |
| Applicant | OSTEOMED 3885 ARAPAHO ROAD Addison, TX 75001 |
| Contact | Blesson Abraham |
| Correspondent | Blesson Abraham OSTEOMED 3885 ARAPAHO ROAD Addison, TX 75001 |
| Product Code | HWC |
| CFR Regulation Number | 888.3040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-02-04 |
| Decision Date | 2014-02-28 |
| Summary: | summary |