510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K211303Substantially Equivalent

Avon Patello-femoral Joint Prosthesis

Howmedica Osteonics Corp., dba Stryker Orthopaedics, Mahwah NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K211303 is the FDA 510(k) clearance record for Avon Patello-femoral Joint Prosthesis, a class II device, cleared for Howmedica Osteonics Corp., Dba Stryker Orthopaedics on under FDA product code KRR (Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer). FDA records list 33 510(k) clearances for Howmedica Osteonics Corp., Dba Stryker Orthopaedics, from to . As of , FDA records show no recalls naming K211303.

Clearance record

Decision date
Received
(36 days to decision)
Product code
KRR Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer
Regulation
21 CFR 888.3540
Device class
Class II
Review panel
Orthopedic
Applicant
Howmedica Osteonics Corp., Dba Stryker Orthopaedics 325 Corporate Dr., Mahwah NJ
510(k) summary
Summary PDF
Third party review
No

Clearances, product code KRR

Trailing 12 months

FDA records hold no clearances under product code KRR in the trailing twelve months.

FDA records show no clearances under product code KRR in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KRR, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260