Cleared Traditional

K972219 - ORTHOPEDIC PLATE SYSTEM

K972219 is the FDA 510(k) clearance for ORTHOPEDIC PLATE SYSTEM by Ferguson Medical. It is a Class 2 Orthopedic device (product code HRS) cleared through the Traditional 510(k) pathway after a 161-day FDA review.

K972219 · Ferguson Medical · Orthopedic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Nov 1997
Decision
161d
Days
Class 2
Risk

K972219 is an FDA 510(k) clearance for the ORTHOPEDIC PLATE 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 Ferguson Medical (Chico, US). The FDA issued a Cleared decision on November 20, 1997 after a review of 161 days - an extended review 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Orthopedic review framework, consistent with the majority of Class II 510(k) submissions.

View all Ferguson Medical devices

Submission Details

510(k) Number K972219 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 12, 1997
Decision Date November 20, 1997
Days to Decision 161 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
39d slower than avg
Panel avg: 122d · This submission: 161d
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 932
Devices cleared under the same product code (HRS) and FDA review panel - the closest regulatory comparables to K972219.
TIMESH SYSTEM
K974017 · Sofamor Danek USA,Inc. · Jan 1998
ORBITAL RECONSTRUCTION PLATES
K973982 · Howmedica, Inc. · Jan 1998
OSTEO BOS SYSTEM PRODUCT LINE EXTENSION
K973438 · Osteonics Corp. · Dec 1997
OSTEO BOS SYSTEM IN STAINLESS STEEL
K973204 · Osteonics Corp. · Sep 1997
ALTA PLATING SYSTEM
K972479 · Howmedica Corp. · Sep 1997
BONE PLATE WITH CABLES
K972223 · Pioneer Surgical Technology · Sep 1997