Cleared Traditional

K183011 - Additive Orthopaedics Patient Specific ...

K183011 is the FDA 510(k) clearance for Additive Orthopaedics Patient Specific ... by Additive Orthopaedics. It is a Class 2 Orthopedic device (product code HRS) cleared through the Traditional 510(k) pathway after a 71-day FDA review.

K183011 · Additive Orthopaedics · Orthopedic device
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Jan 2019
Decision
71d
Days
Class 2
Risk

K183011 is an FDA 510(k) clearance for the Additive Orthopaedics Patient Specific 3D Locking Lattice Plates. Classified as Plate, Fixation, Bone within the HRS classification (a category comprising bone fixation plates and orthopedic hardware), Class II - Special Controls.

Submitted by Additive Orthopaedics (Monmouth Beach, US). The FDA issued a Cleared decision on January 10, 2019 after a review of 71 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 Additive Orthopaedics devices

Submission Details

510(k) Number K183011 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 31, 2018
Decision Date January 10, 2019
Days to Decision 71 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
51d faster than avg
Panel avg: 122d · This submission: 71d
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 885
Devices cleared under the same product code (HRS) and FDA review panel - the closest regulatory comparables to K183011.
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K182810 · Miami Device Solutions, LLC · Dec 2018