Cleared Traditional

K896105 - EVOLUTION HIP SYSTEM

K896105 is an FDA 510(k) clearance for EVOLUTION HIP SYSTEM, manufactured by Dow Corning Wright. The device is a Class 2 Orthopedic device with product code KWL cleared through the Traditional 510(k) pathway after a 70-day FDA review.

K896105 · Dow Corning Wright · Orthopedic device
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Dec 1989
Decision
70d
Days
Class 2
Risk

K896105 is an FDA 510(k) clearance for the EVOLUTION HIP SYSTEM. Classified as Prosthesis, Hip, Hemi-, Femoral, Metal (product code KWL), Class II - Special Controls.

Submitted by Dow Corning Wright (Arlington, US). The FDA issued a Cleared decision on December 29, 1989 after a review of 70 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3360 - 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 Dow Corning Wright devices

FDA 510(k) Submission Details - K896105

510(k) Number K896105 FDA.gov
FDA Decision Cleared Substantially Equivalent - NSE Converted (SN)
Date Received October 20, 1989
Decision Date December 29, 1989
Days to Decision 70 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
52d faster than avg
Panel avg: 122d · This submission: 70d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KWL Device Classification - Class 2, Special Controls

Product Code KWL Prosthesis, Hip, Hemi-, Femoral, Metal
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3360
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 - KWL Prosthesis, Hip, Hemi-, Femoral, Metal

All 77
Devices cleared under the same product code (KWL) and FDA review panel - the closest regulatory comparables to K896105.
THOMPSON TYPE HIS PROSTHESIS
K903240 · Onyx Medical Corp. · Jul 1990
AUSTIN MOORE TYPE HIP PROSTHESIS
K903241 · Onyx Medical Corp. · Jul 1990
PRECISION OSTEOLOCK FEMORAL COMP. TITANIUM PLASMA
K896853 · Howmedica Corp. · May 1990
BIOPRO HEMI-ENDO MODULAR HEAD FOR PSL SYSTEM
K895886 · Biopro, Inc. · Dec 1989
AML(R) COLLARLESS LATERALIZED FEMORAL HIP
K891482 · Depuy, Inc. · May 1989
HIP FRACTURE STEM SYSTEM
K883179 · Howmedica Corp. · Sep 1988