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 |