Cleared Traditional

K063020 - INTAI BONE PLATE AND BONE SCREW SYSTEM

Also marketed or referenced as:
INTAI DHS/DCS PLATE SYSTEM

K063020 is an FDA 510(k) clearance for INTAI BONE PLATE AND BONE SCREW SYSTEM, manufactured by Intai Technology, Inc.. The device is a Class 2 Orthopedic device with product code HRS cleared through the Traditional 510(k) pathway after a 73-day FDA review.

K063020 · Intai Technology, Inc. · Orthopedic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Dec 2006
Decision
73d
Days
Class 2
Risk

K063020 is an FDA 510(k) clearance for the INTAI BONE PLATE AND BONE SCREW SYSTEM. Classified as Plate, Fixation, Bone within the HRS classification (a category comprising bone fixation plates and orthopedic hardware), Class II - Special Controls.

Submitted by Intai Technology, Inc. (Ontario, US). The FDA issued a Cleared decision on December 14, 2006 after a review of 73 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 Intai Technology, Inc. devices

FDA 510(k) Submission Details - K063020

510(k) Number K063020 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 02, 2006
Decision Date December 14, 2006
Days to Decision 73 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
49d faster than avg
Panel avg: 122d · This submission: 73d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HRS Device Classification - Class 2, Special Controls

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 1085
Devices cleared under the same product code (HRS) and FDA review panel - the closest regulatory comparables to K063020.
HUMERUS LOCKING PLATING SYSTEM
K063095 · Newclip Technics · Dec 2006
SYNTHES (USA) MODULAR MINI FRAGMENT LCP SYSTEM
K063049 · Synthes (Usa) · Dec 2006
LORENZ STERNAL CLOSURE SYSTEM
K063506 · Walter Lorenz Surgical, Inc. · Dec 2006
ACUMED CONGRUENT BONE PLATE SYSTEM
K063460 · Acumed, LLC · Dec 2006
UNIVERSAL LOCKING SYSTEM, 2.7MM PLATES & SCREWS
K063303 · Zimmer, Inc. · Nov 2006
PROFYLE SYSTEM
K062498 · Howmedica Osteonics Corp. · Oct 2006