Cleared Traditional

K070695 - ZIMMER PATELLOFEMORAL JOINT PROSTHESIS

K070695 is an FDA 510(k) clearance for ZIMMER PATELLOFEMORAL JOINT PROSTHESIS, manufactured by Zimmer, Inc.. The device is a Class 2 Orthopedic device with product code KRR cleared through the Traditional 510(k) pathway after a 86-day FDA review.

K070695 · Zimmer, Inc. · Orthopedic device
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Jun 2007
Decision
86d
Days
Class 2
Risk

K070695 is an FDA 510(k) clearance for the ZIMMER PATELLOFEMORAL JOINT PROSTHESIS. Classified as Prosthesis, Knee, Patello/femoral, Semi-constrained, Cemented, Metal/polymer (product code KRR), Class II - Special Controls.

Submitted by Zimmer, Inc. (Warsaw, US). The FDA issued a Cleared decision on June 7, 2007 after a review of 86 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3540 - 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 Zimmer, Inc. devices

FDA 510(k) Submission Details - K070695

510(k) Number K070695 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 13, 2007
Decision Date June 07, 2007
Days to Decision 86 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
36d faster than avg
Panel avg: 122d · This submission: 86d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KRR Device Classification - Class 2, Special Controls

Product Code KRR Prosthesis, Knee, Patello/femoral, Semi-constrained, Cemented, Metal/polymer
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3540
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 - KRR Prosthesis, Knee, Patello/femoral, Semi-constrained, Cemented, Metal/polymer

All 25
Devices cleared under the same product code (KRR) and FDA review panel - the closest regulatory comparables to K070695.
MAKO SURGICAL CORP. PATELLOFEMORAL KNEE IMPLANT SYSTEM
K080029 · Mako Surgical Corp. · May 2008
ACCIN PATELLOFEMORAL SYSTEM
K073120 · Accelerated Innovation, LLC · Feb 2008
HEMICAP PATELLO-FEMORAL RESURFACING SYSTEM
K071413 · Arthrosurface, Inc. · Nov 2007
HEMICAP PATELLO-FEMORAL RESURFACING PROSTHESIS
K060127 · Arthrosurface, Inc. · Mar 2006
RBK PATELLA FEMORAL KNEE
K050473 · Global Orthopaedic Technology, USA, Inc. · Nov 2005
AVON PATELLO-FEMORAL JOINT PROSTHESIS
K051948 · Howmedica Osteonics Corp. · Oct 2005