The following data is part of a premarket notification filed by Orthofix Srl with the FDA for Orthofix Galaxy Fixation System.
Device ID | K113770 |
510k Number | K113770 |
Device Name: | ORTHOFIX GALAXY FIXATION SYSTEM |
Classification | Appliance, Fixation, Nail/blade/plate Combination, Multiple Component |
Applicant | ORTHOFIX SRL 15058 ARMEL DR. Oregon City, OR 97045 |
Contact | Candace F Cederman |
Correspondent | Candace F Cederman ORTHOFIX SRL 15058 ARMEL DR. Oregon City, OR 97045 |
Product Code | KTT |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-12-22 |
Decision Date | 2012-09-04 |
Summary: | summary |