OpenLoc-L Spinal Fixation System, LnK Spinal Fixation System
K-Number: K171813 · 2017-07-13
Device Summary
Frequently Asked Questions
What is the OpenLoc-L Spinal Fixation System, LnK Spinal Fixation System?
OpenLoc-L Spinal Fixation System, LnK Spinal Fixation System is a medical device that received FDA 510(k) clearance on 2017-07-13. The listed applicant is L&K BIOMED Co., Ltd.. The 510(k) number is K171813.
When did OpenLoc-L Spinal Fixation System, LnK Spinal Fixation System receive FDA 510(k) clearance?
OpenLoc-L Spinal Fixation System, LnK Spinal Fixation System received FDA 510(k) clearance on 2017-07-13, under 510(k) number K171813.
Who is the listed applicant for OpenLoc-L Spinal Fixation System, LnK Spinal Fixation System?
The FDA 510(k) record lists L&K BIOMED Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OpenLoc-L Spinal Fixation System, LnK Spinal Fixation System?
The FDA product code for OpenLoc-L Spinal Fixation System, LnK Spinal Fixation System is NKB.
Other records listing L&K BIOMED Co., Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: NKB)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.