FDA 510(k) FDA class 2 Substantially Equivalent 🇦🇺 Australia

Field Orthopaedics Bony Trauma Extremity System (BTES) Plate Range and Plate Screws; Field Orthopaedics Bony Trauma Extremity System (BTES) Screw Range

K Number: K200043 · Decision Mar 23, 2020
Classifications
1
FEI Numbers
519
Registration Numbers
519
Same Product Code
1313
Applicant Total
3
Review Days
75

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Basic Information

Device Name
Field Orthopaedics Bony Trauma Extremity System (BTES) Plate Range and Plate Screws; Field Orthopaedics Bony Trauma Extremity System (BTES) Screw Range
K Number
K200043
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Field Orthopaedics Pty, Ltd.
Date Received
January 8, 2020
Decision Date
March 23, 2020
Product Code
HRS
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
HRS Plate, Fixation, Bone

Similar 510(k) Clearances

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

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Other Clearances by Field Orthopaedics Pty, Ltd.

K Number Device Name
K230118 Bony Trauma Extremity System (BTES) Screw Range, NX Nail
K180348 Field Orthopaedics Micro Screw System