The following data is part of a premarket notification filed by Globus Medical Inc. with the FDA for Arbor External Fixation System.
Device ID | K172438 |
510k Number | K172438 |
Device Name: | ARBOR External Fixation System |
Classification | Appliance, Fixation, Nail/blade/plate Combination, Multiple Component |
Applicant | Globus Medical Inc. 2560 General Armistead Ave. Audubon, PA 19403 |
Contact | Kelly J. Baker |
Correspondent | Kelly J. Baker Globus Medical Inc. 2560 General Armistead Ave. Audubon, PA 19403 |
Product Code | KTT |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-08-11 |
Decision Date | 2018-01-12 |
Summary: | summary |