The following data is part of a premarket notification filed by Ewoosoft Co., Ltd with the FDA for Ezortho V1.3.
| Device ID | K220003 |
| 510k Number | K220003 |
| Device Name: | EzOrtho V1.3 |
| Classification | System, Image Processing, Radiological |
| Applicant | Ewoosoft Co., Ltd 801-ho, Vatechnetworks Bldg., 13, Samsung 1-ro 2-gil Hwaseong-si, KR 18449 |
| Contact | Young Seok Kim |
| Correspondent | Priscilla Chung LK Consulting Group USA, Inc. 18881 Von Karman Ave. STE 160 Irvine, CA 92612 |
| Product Code | LLZ |
| CFR Regulation Number | 892.2050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2022-01-04 |
| Decision Date | 2022-02-23 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 08800019700319 | K220003 | 000 |