510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K780763Substantially Equivalent

Entrax Traction Unit

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

K780763 is the FDA 510(k) clearance record for ENTRAX TRACTION UNIT, a class I device, cleared for Orthopedic Equipment Co., Inc. on under FDA product code HSR (Unit, Traction, Hip, Non-Powered, Non-Penetrating). FDA records list 45 510(k) clearances for Orthopedic Equipment Co., Inc., from to . As of , FDA records show no recalls naming K780763.

Clearance record

Decision date
Received
(8 days to decision)
Product code
HSR Unit, Traction, Hip, Non-Powered, Non-Penetrating
Regulation
21 CFR 888.5890
Device class
Class I
Review panel
Orthopedic
Applicant
Orthopedic Equipment Co., Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code HSR

Trailing 12 months

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

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