The following data is part of a premarket notification filed by U&i Corp. with the FDA for Optima Spinal System.
Device ID | K051971 |
510k Number | K051971 |
Device Name: | OPTIMA SPINAL SYSTEM |
Classification | Appliance, Fixation, Spinal Intervertebral Body |
Applicant | U&I CORP. 529-1 YONGHYUN-DONG Euijungbu, Kyunggi-do, KR 480-050 |
Contact | Betty Lim |
Correspondent | Betty Lim U&I CORP. 529-1 YONGHYUN-DONG Euijungbu, Kyunggi-do, KR 480-050 |
Product Code | KWQ |
Subsequent Product Code | MNH |
Subsequent Product Code | MNI |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-07-21 |
Decision Date | 2005-08-04 |
Summary: | summary |