TRILEAP Plating System
K-Number: K253178 · 2026-01-06
ApplicantCrossroads Extremity Systems
Decision Date2026-01-06
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
TRILEAP Plating System is a medical device manufactured by Crossroads Extremity Systems. It received FDA 510(k) clearance on 2026-01-06 under approval number K253178. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the TRILEAP Plating System?
TRILEAP Plating System is a medical device that received FDA 510(k) clearance on 2026-01-06. It is manufactured by Crossroads Extremity Systems. The 510(k) number is K253178.
When was TRILEAP Plating System approved by the FDA?
TRILEAP Plating System received FDA 510(k) clearance on 2026-01-06, under approval number K253178.
What company makes TRILEAP Plating System?
TRILEAP Plating System is manufactured by Crossroads Extremity Systems.
What is the FDA product code for TRILEAP Plating System?
The FDA product code for TRILEAP Plating System is HRS.
Other Devices by Crossroads Extremity Systems
Related Devices (Code: HRS)
K163086VLP MINI-MOD 2.0mm Column PlatesSmith & Nephew, Inc.
K162829Medline UNITE® Ankle Fracture Plating SystemMedline Industries, Inc.
K162974Biomet Microfixation RibFix Blu Thoracic Fixation SystemBiomet Microfixation
K163007Biomet Microfixation SternaLock 360 Sternal Closure SystemBiomet Microfixation
K161696aap LOQTEQ® Distal Lateral Humerus Plate 2.7/3.5Aap Implantate AG
K161747LOQTEQ® VA Distal Tibia Plate System: LOQTEQ® VA Distal Medial Tibia Plate 3.5; LOQTEQ® VA Distal Anterolateral Tibia Plate 3.5; LOQTEQ® VA Distal Fibula Plate 2.7/3.5Aap Implantate AG
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.