Cleared Traditional

K910010 - Q SYSTEM 28 HIP STEM

K910010 is an FDA 510(k) clearance for Q SYSTEM 28 HIP STEM, manufactured by Turnkey Intergration USA, Inc.. The device is a Class 2 Orthopedic device with product code LWJ cleared through the Traditional 510(k) pathway after a 69-day FDA review.

K910010 · Turnkey Intergration USA, Inc. · Orthopedic device
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Mar 1991
Decision
69d
Days
Class 2
Risk

K910010 is an FDA 510(k) clearance for the Q SYSTEM 28 HIP STEM. Classified as Prosthesis, Hip, Semi-constrained, Metal/polymer, Uncemented (product code LWJ), Class II - Special Controls.

Submitted by Turnkey Intergration USA, Inc. (Indianapolis, US). The FDA issued a Cleared decision on March 12, 1991 after a review of 69 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 Turnkey Intergration USA, Inc. devices

FDA 510(k) Submission Details - K910010

510(k) Number K910010 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 02, 1991
Decision Date March 12, 1991
Days to Decision 69 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
53d faster than avg
Panel avg: 122d · This submission: 69d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

LWJ Device Classification - Class 2, Special Controls

Product Code LWJ Prosthesis, Hip, Semi-constrained, Metal/polymer, Uncemented
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 - LWJ Prosthesis, Hip, Semi-constrained, Metal/polymer, Uncemented

All 62
Devices cleared under the same product code (LWJ) and FDA review panel - the closest regulatory comparables to K910010.
VENUS HIP
K913708 · Turnkey Intergration USA, Inc. · Jan 1992
TI-FIT FEMORAL COMPONENT
K914343 · Smith & Nephew Richards, Inc. · Jan 1992
HOWMEDICA HNR SYSTEM
K903563 · Howmedica Corp. · Mar 1991
THACKRAY ORTHOGENESIS IDENTIFIT FEMORAL HIP PROSTH
K905254 · Depuy, Inc. · Feb 1991
GERI TOTAL HIP SYSTEM
K905186 · Smith & Nephew Richards, Inc. · Feb 1991
ACSYS SELFTAP ACETABULAR CUP PROSTHESIS
K900262 · 3M Company · Sep 1990