Medartis AG
FDA 510(k) medical device clearances.
Top product codes for Medartis AG
Recent clearances by Medartis AG
- K260761 — APTUS Clavicle System 2.8
- K260934 — TITAN Nail; APTUS K-Wire System
- K253916 — APTUS Shoulder Proximal Humerus System, PentaLock 3.5
- K243610 — APTUS Hand System; APTUS Elbow Dorsal Olecranon
- K240613 — APTUS Elbow Dorsal Olecranon Plates
- K232105 — APTUS Foot System 2.8-3.5
- K234062 — APTUS Hand Scaphoid Plates
- K232251 — APTUS Cannulated Compression Screws Line Extension, APTUS K-Wire System Line Extension
- K232144 — Sterile Products of the APTUS System
- K230971 — APTUS® 3.5 TriLock Straight Plates
- K223853 — Medartis APTUS® Ulna Plates
- K202589 — APTUS Cannulated Compression Screws, APTUS headed Cannulated Compression Screws, APTUS K-Wire System
- K193633 — APTUS® Ankle Trauma System 2.8/3.5
- K193639 — APTUS® Foot 2.8-3.5 System
- K193554 — APTUS® Forearm Shaft Plates and APTUS® Wrist 2.5 System
- K192984 — APTUS Clavicle System
- K192297 — APTUS Wrist Arthrodesis Plates
- K191848 — APTUS Wrist Spanning Plates 2.5
- K191636 — APTUS Foot System
- K181009 — APTUS CMC-I Fusion Plate System
- K181425 — APTUS® Proximal Humerus System
- K172170 — APTUS(R) Wrist 2.5 System
- K161861 — APTUS® Coronoid 2.0
- K142906 — APTUS Wrist 2.5 System
- K142581 — APTUS Foot System
- K141232 — APTUS ULNA SHORTENING 2.5
- K133460 — APTUS CANNULATED COMPRESSION SCREWS
- K120108 — APTUS PROXIMAL HUMERUS SYSTEM
- K112169 — APTUS WRIST ARTHRODESIS PLATES
- K112560 — APTUS(R) DISTAL HUMERUS SYSTEM
- K110908 — APTUS FOOT 3.5 SYSTEM
- K110658 — APTUS CANNULATED COMPRESSION SCREWS
- K103332 — APTUS ULNA PLATES
- K102537 — APTUS 1.5 TRILOCK
- K092038 — APTUS K-WIRE SYSTEM
- K091479 — APTUS FOOT SYSTEM
- K090983 — APTUS 2.0/2.3 FOUR CORNER FUSION PLATE
- K090053 — APTUS 2.0 RADIAL HEAD SYSTEM
- K071612 — MODUS TRILOCK 2.0/2.3/2.5
- K992682 — MODUS 2.5 MANDIBULAR RECONSTRUCTION SET
- K992683 — MODUS 2.5 MANDIBULAR TRAUMA SET
- K992106 — MODUS SYSTEM SELF-DRILLING SCREWS
Data sourced from openFDA. This site is unofficial and independent of the FDA.