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 |