Cleared Traditional

K071723 - ZIMMER POROLOCK MIS STEM

K071723 is the FDA 510(k) clearance for ZIMMER POROLOCK MIS STEM by Zimmer GmbH. It is a Class 3 Orthopedic device (product code KWA) cleared through the Traditional 510(k) pathway after a 256-day FDA review.

K071723 · Zimmer GmbH · Orthopedic device
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Mar 2008
Decision
256d
Days
Class 3
Risk

K071723 is an FDA 510(k) clearance for the ZIMMER POROLOCK MIS STEM. Classified as Prosthesis, Hip, Semi-constrained (metal Uncemented Acetabular Component) (product code KWA), Class III - Premarket Approval.

Submitted by Zimmer GmbH (Warsaw, US). The FDA issued a Cleared decision on March 7, 2008 after a review of 256 days - an extended review cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3330 - 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. High regulatory complexity profile. 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 Zimmer GmbH devices

Submission Details

510(k) Number K071723 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 25, 2007
Decision Date March 07, 2008
Days to Decision 256 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
134d slower than avg
Panel avg: 122d · This submission: 256d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code KWA Prosthesis, Hip, Semi-constrained (metal Uncemented Acetabular Component)
Device Class Class 3 - Premarket Approval
CFR Regulation 21 CFR 888.3330
What this classification means

Class III devices typically require Premarket Approval (PMA) with clinical evidence. Clearance through 510(k) for Class III devices is granted only when substantial equivalence to a valid predicate can be established.

Regulatory Peers - KWA Prosthesis, Hip, Semi-constrained (metal Uncemented Acetabular Component)

All 91
Devices cleared under the same product code (KWA) and FDA review panel - the closest regulatory comparables to K071723.
ZIMMER M/L TAPER HIP PROSTHESIS WITH KINECTIV TECHNOLOGY SYSTEM
K081007 · Zimmer, Inc. · May 2008
PROFEMUR LX REVISION 5/8 COATED HIP STEM
K080663 · Wrightmedicaltechnologyinc · Apr 2008
PARALLEL-SIDED EXTENSIVELY COATED FEMORAL STEMS
K073637 · Biomet Manufacturing Corp · Mar 2008
DEPUY ASR 300 ACETABULAR CUP SYSTEM
K073413 · DePuy Orthopaedics, Inc. · Jan 2008
ZIMMER M/L TAPER HIP PROSTHESIS WITH KINECTIV TECHNOLOGY SYSTEM, MODEL(S) 7848 SERIES( MODULAR NECKS), 7713 SERIES
K071856 · Zimmer, Inc. · Jul 2007
FMP METAL/METAL ACETABULAR INSERT, 499-28,449-34, 499-38
K070221 · Encore Medical, L.P. · Apr 2007