Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

AAP LOQTEQ PROXIMAL LATERAL TIBIA PLATE 4.5 SYSTEM

K-Number: K113602 · 2012-10-31

ApplicantAap Implantate AG
Decision Date2012-10-31
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

AAP LOQTEQ PROXIMAL LATERAL TIBIA PLATE 4.5 SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Aap Implantate AG. It received FDA 510(k) clearance on 2012-10-31 under 510(k) number K113602. 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 AAP LOQTEQ PROXIMAL LATERAL TIBIA PLATE 4.5 SYSTEM?

AAP LOQTEQ PROXIMAL LATERAL TIBIA PLATE 4.5 SYSTEM is a medical device that received FDA 510(k) clearance on 2012-10-31. The listed applicant is Aap Implantate AG. The 510(k) number is K113602.

When did AAP LOQTEQ PROXIMAL LATERAL TIBIA PLATE 4.5 SYSTEM receive FDA 510(k) clearance?

AAP LOQTEQ PROXIMAL LATERAL TIBIA PLATE 4.5 SYSTEM received FDA 510(k) clearance on 2012-10-31, under 510(k) number K113602.

Who is the listed applicant for AAP LOQTEQ PROXIMAL LATERAL TIBIA PLATE 4.5 SYSTEM?

The FDA 510(k) record lists Aap Implantate AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AAP LOQTEQ PROXIMAL LATERAL TIBIA PLATE 4.5 SYSTEM?

The FDA product code for AAP LOQTEQ PROXIMAL LATERAL TIBIA PLATE 4.5 SYSTEM is HRS.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Aap Implantate AG 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.

K254253LOQTEQ® VA Proximal Humerus Plate 3.5K233008Cannulated Headless Bone ScrewsK230141LOQTEQ® VA Elbow Plates 2.7/3.5 SystemK211582LOQTEQ Proximal Humerus Plate 3.5 SystemK210043LOQTEQ Distal Lateral Femur Plate 4.5 SystemK182818LOQTEQ VA Calcaneus Plate 3.5

View all 32 devices →

Related Devices (Code: HRS)

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.

K261892ProRib Fixation SystemCosta Surgical, Inc.K262098EnHAnce PEEK Bunion SystemNvision Biomedical TechnologiesK262963TMC Implant Fixation SystemTreace Medical Concepts, Inc.K261647Tempo Plating System; Ultra Compression Screw SystemPace SurgicalK261830FRAXION 3.5 Plate System (Various - See Catalog);FRAXION 4.5 Plate System (Various - See Catalog);FRAXION Mini Plate System (Various - See Catalog);FRAXION Bone Screw System (Various - See Catalog)Ortler Global Tibbi Gerecler Anonim SirketiK262537Versalock Sterile Plating SystemGM Dos Reis Industria e Comercio Ltda.

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.

↑