The following data is part of a premarket notification filed by Jeil Medical Corporation with the FDA for Leforte System Ii.
Device ID | K150965 |
510k Number | K150965 |
Device Name: | LeForte System II |
Classification | Plate, Bone |
Applicant | Jeil Medical Corporation 702, 703, 704, 705, 706, 804, 805,807,812-ho ,55, Digital-ro34-gil, Guro-gu Seoul-city, KR 152-728 |
Contact | Jieun Kim |
Correspondent | Priscilla Chung LK Consulting Group USA, Inc. 2651 East Chapman Avenue, Suite 110 Fullerton, CA 92831 |
Product Code | JEY |
CFR Regulation Number | 872.4760 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-04-10 |
Decision Date | 2015-09-17 |
Summary: | summary |