Cleared Traditional

K954712 - INTRAMEDULLARY HIP SCREW (MODIFICATION)

K954712 is the FDA 510(k) clearance for INTRAMEDULLARY HIP SCREW (MODIFICATION) by Smith & Nephew Richards, Inc.. It is a Class 2 Orthopedic device (product code KTT) cleared through the Traditional 510(k) pathway after a 76-day FDA review.

K954712 · Smith & Nephew Richards, Inc. · Orthopedic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Oct 1995
Decision
76d
Days
Class 2
Risk

K954712 is an FDA 510(k) clearance for the INTRAMEDULLARY HIP SCREW (MODIFICATION). Classified as Appliance, Fixation, Nail/blade/plate Combination, Multiple Component (product code KTT), Class II - Special Controls.

Submitted by Smith & Nephew Richards, Inc. (Memphis, US). The FDA issued a Cleared decision on October 31, 1995 after a review of 76 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 Smith & Nephew Richards, Inc. devices

Submission Details

510(k) Number K954712 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 16, 1995
Decision Date October 31, 1995
Days to Decision 76 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
46d faster than avg
Panel avg: 122d · This submission: 76d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code KTT Appliance, Fixation, Nail/blade/plate Combination, Multiple Component
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 - KTT Appliance, Fixation, Nail/blade/plate Combination, Multiple Component

All 287
Devices cleared under the same product code (KTT) and FDA review panel - the closest regulatory comparables to K954712.
OMEGA+ COMPRESSION SCREW SYSTEM
K955306 · Howmedica Corp. · Apr 1996
VERSA-FX FEMORAL FIXATION SYSTEM
K954555 · Zimmer, Inc. · Jan 1996
EBI X FIX DYNAFIX SYSTEM (DFS)
K953406 · Electro-Biology, Inc. · Oct 1995
GLIDING NAIL
K951809 · Encore Orthopedics, Inc. · Jul 1995
EBI SMALL EXTERNAL FIXATOR (S/E/F/)
K951357 · Electro-Biology, Inc. · Jun 1995
DEPUY COMPRESSION HIP SCREW SYSTEM
K946156 · Depuy, Inc. · May 1995