The following data is part of a premarket notification filed by Ortho Solutions Limited with the FDA for Oxford Ankle Fusion Nail(afn) System.
Device ID | K121575 |
510k Number | K121575 |
Device Name: | OXFORD ANKLE FUSION NAIL(AFN) SYSTEM |
Classification | Rod, Fixation, Intramedullary And Accessories |
Applicant | ORTHO SOLUTIONS LIMITED 3150 EAST 200TH STREET Prior Lake, MN 55372 |
Contact | Al Lippincott |
Correspondent | Al Lippincott ORTHO SOLUTIONS LIMITED 3150 EAST 200TH STREET Prior Lake, MN 55372 |
Product Code | HSB |
CFR Regulation Number | 888.3020 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-05-30 |
Decision Date | 2012-09-14 |
Summary: | summary |