510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K801436Substantially Equivalent

Orthopedic Lower Extremity Suspension

Mizuho Orthopedic Systems Inc, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K801436 is the FDA 510(k) clearance record for ORTHOPEDIC LOWER EXTREMITY SUSPENSION, a class I device, cleared for Orthopedic Systems, Inc. on under FDA product code FYH (Splint, Extremity, Noninflatable, External, Sterile). FDA records list 95 510(k) clearances for MIZUHO ORTHOPEDIC SYSTEMS, INC., from to . As of , FDA records show no recalls naming K801436.

Clearance record

Decision date
Received
(7 days to decision)
Product code
FYH Splint, Extremity, Noninflatable, External, Sterile
Regulation
21 CFR 878.3910
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Orthopedic Systems, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code FYH

Trailing 12 months

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

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