Cleared Traditional

K103384 - ESCALADE ACETABULAR CUP SYSTEM

K103384 is an FDA 510(k) clearance for ESCALADE ACETABULAR CUP SYSTEM, manufactured by Ortho Development. The device is a Class 2 Orthopedic device with product code LPH cleared through the Traditional 510(k) pathway after a 118-day FDA review.

K103384 · Ortho Development · Orthopedic device
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Mar 2011
Decision
118d
Days
Class 2
Risk

K103384 is an FDA 510(k) clearance for the ESCALADE ACETABULAR CUP SYSTEM. Classified as Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented (product code LPH), Class II - Special Controls.

Submitted by Ortho Development (Draper, US). The FDA issued a Cleared decision on March 16, 2011 after a review of 118 days - within the typical 510(k) review window.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3358 - 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 Ortho Development devices

FDA 510(k) Submission Details - K103384

510(k) Number K103384 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 18, 2010
Decision Date March 16, 2011
Days to Decision 118 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
4d faster than avg
Panel avg: 122d · This submission: 118d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

LPH Device Classification - Class 2, Special Controls

Product Code LPH Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3358
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 - LPH Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented

All 478
Devices cleared under the same product code (LPH) and FDA review panel - the closest regulatory comparables to K103384.
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