The following data is part of a premarket notification filed by Osteomed L.p. with the FDA for Osteomed Headless Cannulated Screw System.
| Device ID | K063298 |
| 510k Number | K063298 |
| Device Name: | OSTEOMED HEADLESS CANNULATED SCREW SYSTEM |
| Classification | Screw, Fixation, Bone |
| Applicant | OSTEOMED L.P. 3885 ARAPAHO RD. Addison, TX 75001 |
| Contact | Dawn D Tindall |
| Correspondent | Dawn D Tindall OSTEOMED L.P. 3885 ARAPAHO RD. Addison, TX 75001 |
| Product Code | HWC |
| CFR Regulation Number | 888.3040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-11-01 |
| Decision Date | 2007-03-02 |
| Summary: | summary |