The following data is part of a premarket notification filed by U&i Corp. with the FDA for Dyna Locking Cannulated Screw.
Device ID | K112240 |
510k Number | K112240 |
Device Name: | DYNA LOCKING CANNULATED SCREW |
Classification | Screw, Fixation, Bone |
Applicant | U&I CORP. 529-1 YONGHYN-DONG Uijungbu, Kyunggi-do, KR 480-050 |
Contact | Gyeong-je Kwon |
Correspondent | Gyeong-je Kwon U&I CORP. 529-1 YONGHYN-DONG Uijungbu, Kyunggi-do, KR 480-050 |
Product Code | HWC |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-08-04 |
Decision Date | 2012-01-04 |
Summary: | summary |