Cleared Traditional

K920524 - OSTEONICS 7000 SERIES TOTAL KNEE BONE AUGMENTATION

K920524 is an FDA 510(k) clearance for OSTEONICS 7000 SERIES TOTAL KNEE BONE A..., manufactured by Osteonics Corp.. The device is a Class 2 Orthopedic device with product code JWH cleared through the Traditional 510(k) pathway after a 100-day FDA review.

K920524 · Osteonics Corp. · Orthopedic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
May 1992
Decision
100d
Days
Class 2
Risk

K920524 is an FDA 510(k) clearance for the OSTEONICS 7000 SERIES TOTAL KNEE BONE AUGMENTATION. Classified as Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer (product code JWH), Class II - Special Controls.

Submitted by Osteonics Corp. (Allendale, US). The FDA issued a Cleared decision on May 15, 1992 after a review of 100 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 Osteonics Corp. devices

FDA 510(k) Submission Details - K920524

510(k) Number K920524 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 05, 1992
Decision Date May 15, 1992
Days to Decision 100 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
22d faster than avg
Panel avg: 122d · This submission: 100d
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 893
Devices cleared under the same product code (JWH) and FDA review panel - the closest regulatory comparables to K920524.
PSK FEMORAL AND TIBIAL INSERT COMPONENT
K920426 · Orthomet, Inc. · Aug 1992
FEMORAL AND ALL POLY TIBIAL TRAY COMPONENTS
K920698 · Orthomet, Inc. · Aug 1992
OSTEONICS 7000 POSTERIOR STAB. TOTAL KNEE FEM. COM
K914565 · Osteonics Corp. · May 1992
CONTINUUM KNEE SYSTEM (CKS)
K914072 · Techmedica, Inc. · Feb 1992
7000 SERIES TOTAL KNEE PATELLAR COMPONENTS
K915186 · Osteonics Corp. · Feb 1992
7000 SERIES MODULAR TIBIAL COMPONENTS
K915192 · Osteonics Corp. · Feb 1992