The following data is part of a premarket notification filed by Warsaw Orthopedic, Inc. with the FDA for Supracondylar Bone Plate.
| Device ID | K851919 |
| 510k Number | K851919 |
| Device Name: | SUPRACONDYLAR BONE PLATE |
| Classification | Appliance, Fixation, Nail/blade/plate Combination, Multiple Component |
| Applicant | WARSAW ORTHOPEDIC, INC. P.O. BOX 1157 Warsaw, IN 46580 |
| Contact | James Ritter |
| Correspondent | James Ritter WARSAW ORTHOPEDIC, INC. P.O. BOX 1157 Warsaw, IN 46580 |
| Product Code | KTT |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-05-02 |
| Decision Date | 1985-06-28 |