Product code KRR— Orthopedic
AVON PATELLO-FEMORAL JOINT PROSTHESIS
- Classification name
- Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer
- Device class
- Class 2
- Regulation
- 21 CFR 888.3540
- Advisory panel
- Orthopedic
- Total cleared
- 27
- First cleared
- Most recent
Market context for product code KRR
FDA has cleared devices under product code KRR between 1996 and 2023, filed by 20 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Clearances per year
last 15 years- 2023
- 2022
- 2021
- 2020
- 2018
- 2016
- 2015
- 2013
- 2012
- 2008
- 2007
- 2006
- 2005
- 2004
- 2002
Top applicants under product code KRR
Recent clearances under product code KRR
- K231253 — Overture Orthopaedics Patellofemoral System
- K221048 — Episealer Patellofemoral System
- K211303 — Avon Patello-femoral Joint Prosthesis
- K200122 — MOTO PFJ System
- K181280 — Patello-Femoral Wave (Kahuna) Arthroplasty System
- K160461 — Arthrex iBalance BiCompartmental Arthroplasty System
- K143543 — Prelude PF Patellae
- K123907 — PRELUDE PF FEMORAL COMPONENTS (MIM COCRMO), PRELUDE PF FEMORAL COMPONENTS (CAST COCRMO), PRELUDE PF PATELLA COMPONENTS,
- K111970 — KNEETEC PFJ&HLS KNEETEC PATELLAR COMPONENT
- K082088 — MAKO SURGICAL CORP. PATELLOFEMORAL KNEE IMPLANT SYSTEM II
- K080029 — MAKO SURGICAL CORP. PATELLOFEMORAL KNEE IMPLANT SYSTEM
- K073120 — ACCIN PATELLOFEMORAL SYSTEM
- K071413 — HEMICAP PATELLO-FEMORAL RESURFACING SYSTEM
- K070695 — ZIMMER PATELLOFEMORAL JOINT PROSTHESIS
- K060127 — HEMICAP PATELLO-FEMORAL RESURFACING PROSTHESIS
- K050473 — RBK PATELLA FEMORAL KNEE
- K051948 — AVON PATELLO-FEMORAL JOINT PROSTHESIS
- K051086 — SMITH & NEPHEW PATELLO-FEMORAL IMPLANT
- K041160 — AVON EXTRA-SMALL PATELLO-FEMORAL REPLACEMENT
- K013982 — KINEMATCH PATELLO-FEMORAL RESURFACING IMPALANT
- K020841 — AVON PATELLAR COMPONENT
- K010100 — AVON PATELLO-FEMORAL JOINT PROSTHESIS
- K002356 — NATURAL-KNEE II PATELLOFEMORAL JOINT PROSTHESIS
- K001374 — PATIENT MATCHED COBALT ALLOY TROCHLEA REPLACEMENT
- K001350 — PATIENT MATCHED TITANIUM ALLOY TROCHLEA
- K000827 — UNICOMPARTMENTAL PATELLOFEMORAL PROSTHESIS (UPP) CEMENTED
- K962190 — PATELLOFEMORAL JOINT PROSTHESIS
Data sourced from openFDA. This site is unofficial and independent of the FDA.