Cleared Traditional

K893762 - PLUS TOTAL KNEE SYSTEM

K893762 is an FDA 510(k) clearance for PLUS TOTAL KNEE SYSTEM, manufactured by Orthomet, Inc.. The device is a Class 2 Orthopedic device with product code JWH cleared through the Traditional 510(k) pathway after a 119-day FDA review.

K893762 · Orthomet, Inc. · Orthopedic device
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Sep 1989
Decision
119d
Days
Class 2
Risk

K893762 is an FDA 510(k) clearance for the PLUS TOTAL KNEE SYSTEM, (PPD) TIBIAL COMPONENT. Classified as Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer (product code JWH), Class II - Special Controls.

Submitted by Orthomet, Inc. (Minneapolis, US). The FDA issued a Cleared decision on September 15, 1989 after a review of 119 days - within the typical 510(k) review window.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3560 - 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 Orthomet, Inc. devices

FDA 510(k) Submission Details - K893762

510(k) Number K893762 FDA.gov
FDA Decision Cleared Substantially Equivalent - NSE Converted (SN)
Date Received May 19, 1989
Decision Date September 15, 1989
Days to Decision 119 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
3d faster than avg
Panel avg: 122d · This submission: 119d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JWH Device Classification - Class 2, Special Controls

Product Code JWH Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3560
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 - JWH Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer

All 800
Devices cleared under the same product code (JWH) and FDA review panel - the closest regulatory comparables to K893762.
KINEMAX TOTAL KNEE SYSTEM FEMORAL SPACERS
K894658 · Howmedica Corp. · Oct 1989
WHITESIDE ORTHOLOC M.A. TIBIAL BASE
K894504 · Dow Corning Wright · Oct 1989
SECOND GENERATION KNEE SYSTEM
K894334 · Orthomet, Inc. · Oct 1989
MG II POROUS TOTAL KNEE SYSTEM
K892800 · Zimmer, Inc. · Aug 1989
WHITESIDE ORTHOLOC M.A. TOTAL KNEE SYSTEM
K893252 · Dow Corning Wright · Jul 1989
POROUS GENESIS PATELLAR AND STEMLESS TIBIAL COMP.
K890132 · Richards Medical Co., Inc. · Jul 1989