The following data is part of a premarket notification filed by Osteomed Lp with the FDA for Extrimilock Ankle Plating System.
| Device ID | K133691 |
| 510k Number | K133691 |
| Device Name: | EXTRIMILOCK ANKLE PLATING SYSTEM |
| Classification | Plate, Fixation, Bone |
| Applicant | OSTEOMED LP 3885 Arapaho Rd Addison, TX 75001 |
| Contact | Blesson Abraham |
| Correspondent | Blesson Abraham OSTEOMED LP 3885 Arapaho Rd Addison, TX 75001 |
| Product Code | HRS |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-12-02 |
| Decision Date | 2014-02-24 |
| Summary: | summary |