510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K870125Substantially Equivalent

Extremity Elevator

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

K870125 is the FDA 510(k) clearance record for EXTREMITY ELEVATOR, a class I device, cleared for Orthopedic Systems, Inc. on under FDA product code HST (Apparatus, Traction, Non-Powered). FDA records list 95 510(k) clearances for MIZUHO ORTHOPEDIC SYSTEMS, INC., from to . As of , FDA records show no recalls naming K870125.

Clearance record

Decision date
Received
(23 days to decision)
Product code
HST Apparatus, Traction, Non-Powered
Regulation
21 CFR 888.5850
Device class
Class I
Review panel
Orthopedic
Applicant
Orthopedic Systems, Inc. 1897 National Ave., Hayward CA
Third party review
No

Clearances, product code HST

Trailing 12 months

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

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