Cleared Traditional

Field Orthopaedics Bony Trauma Extremity System (BTES) Plate Range and Plate Screws (K200043) - FDA 510(k) Clearance

Also marketed or referenced as:
Field Orthopaedics Bony Trauma Extremity System (BTES) Screw Range

Class II Orthopedic device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K200043 · Field Orthopaedics Pty, Ltd. · Orthopedic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 2020
Decision
75d
Days
Class 2
Risk

K200043 is an FDA 510(k) clearance for the Field Orthopaedics Bony Trauma Extremity System (BTES) Plate Range and Plate .... Classified as Plate, Fixation, Bone within the HRS classification (a category comprising bone fixation plates and orthopedic hardware), Class II - Special Controls.

Submitted by Field Orthopaedics Pty, Ltd. (Spring Hill, AU). The FDA issued a Cleared decision on March 23, 2020 after a review of 75 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3030 - the FDA orthopedic device regulatory framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Field Orthopaedics Pty, Ltd. devices

Submission Details

510(k) Number K200043 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 08, 2020
Decision Date March 23, 2020
Days to Decision 75 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
47d faster than avg
Panel avg: 122d · This submission: 75d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code HRS Plate, Fixation, Bone
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3030
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Orthopedic devices follow this clearance model.

Regulatory Peers - HRS Plate, Fixation, Bone

All 700
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