510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K072704Substantially Equivalent

Unicompartmental Knee

Valpo Orthopedic Technology, Inc., Warsaw IN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K072704 is the FDA 510(k) clearance record for UNICOMPARTMENTAL KNEE, a class II device, cleared for Valpo Orthopedic Technology, Inc. on under FDA product code HRY (Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer). FDA records list 2 510(k) clearances for Valpo Orthopedic Technology, Inc., from to . As of , FDA records show no recalls naming K072704.

Clearance record

Decision date
Received
(148 days to decision)
Product code
HRY Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer
Regulation
21 CFR 888.3530
Device class
Class II
Review panel
Orthopedic
Applicant
Valpo Orthopedic Technology, Inc. 438 E 200 N, Warsaw IN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HRY

Trailing 12 months

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

FDA records show no clearances under product code HRY in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HRY, 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