FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇭 Switzerland

APTUS Foot System

K Number: K191636 · Decision Aug 16, 2019
Classifications
1
FEI Numbers
245
Registration Numbers
245
Same Product Code
230
Applicant Total
42
Review Days
58

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
APTUS Foot System
K Number
K191636
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medartis AG
Date Received
June 19, 2019
Decision Date
August 16, 2019
Product Code
JDR
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JDR Staple, Fixation, Bone

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JDR), ordered by most recent decision date.

View all

Other Clearances by Medartis AG

K Number Device Name
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
Search all 42 clearances from Medartis AG →