510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K013982Substantially Equivalent

Kinematch Patello-Femoral Resurfacing Impalant

Kinamed Inc, Camarillo CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K013982 is the FDA 510(k) clearance record for KINEMATCH PATELLO-FEMORAL RESURFACING IMPALANT, a class II device, cleared for Kinamed, Inc. on under FDA product code KRR (Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer). FDA records list 33 510(k) clearances for Kinamed, Inc., from to . As of , FDA records show no recalls naming K013982.

Clearance record

Decision date
Received
(169 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
Kinamed, Inc. 820 Flynn Rd., Camarillo CA
510(k) summary
Statement
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