The following data is part of a premarket notification filed by L & K Biomed Co., Ltd with the FDA for Venus Interbody Fixation System- Venus Plif/tlif, Alif Peek Cage.
Device ID | K110783 |
510k Number | K110783 |
Device Name: | VENUS INTERBODY FIXATION SYSTEM- VENUS PLIF/TLIF, ALIF PEEK CAGE |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
Applicant | L & K BIOMED CO., LTD ROOM 1104, ACE HIGH-END TOWER3 371-50 GASAN-DONG, GEUMCHEON-G Seoul, KR 153803 |
Contact | Hee Kyeong Joo |
Correspondent | Hee Kyeong Joo L & K BIOMED CO., LTD ROOM 1104, ACE HIGH-END TOWER3 371-50 GASAN-DONG, GEUMCHEON-G Seoul, KR 153803 |
Product Code | MAX |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-03-21 |
Decision Date | 2011-10-24 |
Summary: | summary |