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
K813016Substantially Equivalent

Zee Traction Splint

Zee Medical Products Co., Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K813016 is the FDA 510(k) clearance record for ZEE TRACTION SPLINT, a class I device, cleared for Zee Medical Products Co., Inc. on under FDA product code HST (Apparatus, Traction, Non-Powered). FDA records list 8 510(k) clearances for Zee Medical Products Co., Inc., from to . As of , FDA records show no recalls naming K813016.

Clearance record

Decision date
Received
(28 days to decision)
Product code
HST Apparatus, Traction, Non-Powered
Regulation
21 CFR 888.5850
Device class
Class I
Review panel
Orthopedic
Applicant
Zee Medical Products Co., Inc. 803 N. Front St. Suite 3, Mchenry IL
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