510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K221048Substantially Equivalent

Episealer Patellofemoral System

Episurf Medical Inc, New York NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K221048 is the FDA 510(k) clearance record for Episealer Patellofemoral System, a class II device, cleared for Episurf Medical, Inc. on under FDA product code KRR (Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer). FDA records list one 510(k) clearance for Episurf Medical, Inc. As of , FDA records show no recalls naming K221048.

Clearance record

Decision date
Received
(259 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
Episurf Medical, Inc. 220 E 42nd St., Suite 409a, New York NY
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