Atlas FDA

LumFix Spinal Fixation Sytem

FDA 510(k) clearance K160731 · decided 2016-10-04

Clearance details

K-number
K160731
Device name
LumFix Spinal Fixation Sytem
Applicant
CG Bio Co., Ltd.
Decision
Substantially Equivalent
Date received
2016-03-17
Decision date
2016-10-04
Days to decision
201 days
Clearance type
Traditional
Product code
MNI
Device class
2
Regulation number
888.3070
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Seongnam-Si, KR
Third-party review
No
Expedited review
No

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Similar devices under this product code

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RecordFirmDate
Mikron Spinal Fixation System (K171497)Mikron Makina Sanayi Ticaret Co. , Ltd.2017-10-12
Double Medical Universal Spine System (K151458)Double Medical Technology, Inc.2016-08-22
MySpine Pedicle Screw Placement Guides - LP (K153273)Medacta International S.A.2016-06-29
LUMIS Cannulated Pedicle Screw Fixation System, U.L.I.S. Pedicle Screw Fixation System (K160124)Spinevision S.A.2016-04-04
Premier (K160320)Shandong Weigao Orthopaedic Device Co., Ltd.2016-04-01
Sniper (R) Spine System (K160003)Spine Wave, Inc.2016-02-26
YAHUA Spinal System (K152324)Beijing Weigao Yahua Artificial Joint Development Co. , Ltd.2016-02-01
FIREFLY Pedicle Screw Navigation Guide (K143222)Mighty Oak Medical, Inc.2015-12-11
WASTON General Spinal System (K150684)Changzhou Waston Medical Appliance Co., Ltd.2015-11-18
X-spine Pedicle Screw System (K152132)X-Spine Systems, Inc.2015-09-25
Gemmed pedicle screw spinal system (K151592)Suzhou Gemmed Medical Instrument Co., Ltd.2015-09-24
ODALYS Pedicle Screw System (K152098)Kisco International2015-09-17

Recalls involving this device

No recalls on record reference this clearance.