The following data is part of a premarket notification filed by Ortho Solutions Limited with the FDA for Ortho Solutions Extremity Fixation Implants For Osteosysnthesis.
| Device ID | K111678 |
| 510k Number | K111678 |
| Device Name: | ORTHO SOLUTIONS EXTREMITY FIXATION IMPLANTS FOR OSTEOSYSNTHESIS |
| Classification | Plate, Fixation, Bone |
| Applicant | ORTHO SOLUTIONS LIMITED 3150 E. 200TH STREET Prior Lake, MN 55372 |
| Contact | Al Lippincott |
| Correspondent | Al Lippincott ORTHO SOLUTIONS LIMITED 3150 E. 200TH STREET Prior Lake, MN 55372 |
| Product Code | HRS |
| Subsequent Product Code | HWC |
| Subsequent Product Code | JDR |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-06-15 |
| Decision Date | 2012-02-07 |
| Summary: | summary |