Cleared Traditional

K112898 - DELTA TT CUPS, DELTA TT LINERS, BONE SCREWS

K112898 is an FDA 510(k) clearance for DELTA TT CUPS, manufactured by Lima Corporate S.P.A.. The device is a Class 2 Orthopedic device with product code LPH cleared through the Traditional 510(k) pathway after a 445-day FDA review.

K112898 · Lima Corporate S.P.A. · Orthopedic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Dec 2012
Decision
445d
Days
Class 2
Risk

K112898 is an FDA 510(k) clearance for the DELTA TT CUPS, DELTA TT LINERS, BONE SCREWS. Classified as Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented (product code LPH), Class II - Special Controls.

Submitted by Lima Corporate S.P.A. (Winona Lake, US). The FDA issued a Cleared decision on December 21, 2012 after a review of 445 days - an unusually long review period, suggesting complex equivalence evaluation.

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: High-complexity regulatory submission. Elevated predicate reliance profile. The extended review timeline suggests the FDA required additional documentation before confirming substantial equivalence - a pattern common in complex or first-of-kind Orthopedic submissions.

View all Lima Corporate S.P.A. devices

FDA 510(k) Submission Details - K112898

510(k) Number K112898 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 03, 2011
Decision Date December 21, 2012
Days to Decision 445 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
323d slower than avg
Panel avg: 122d · This submission: 445d
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 543
Devices cleared under the same product code (LPH) and FDA review panel - the closest regulatory comparables to K112898.
DEPUY M-SPEC 36MM FEMORAL HEADS
K120599 · Depuy Orthopaedics · Apr 2013
ARCOS TROCHANTER BUTTON
K130063 · Biomet, Inc. · Apr 2013
ORIGIN HIP STEM, FEMORAL HEAD, LOGICAL PX-SERIES ACETABULAR SHELL, LOCIGAL G-SERIES ACETABULAR SHELL, LOGICAL ACETABULAR
K121297 · Signature Orthopaedics Pty, Ltd. · Dec 2012
CS2 HIP SYSTEM
K122512 · Consensus Orthopedics, Inc. · Nov 2012
REVELATION POROUS COATED HIP STEM, SIZE 8
K122636 · Encore Medical, L.P. · Nov 2012
ZENITH, FEMORAL STEM ZENITH, DISTAL CENTRALIZER FOMORAL HEAD ACETABULAR INSERT
K121636 · Tgm Medical, Inc. · Oct 2012