510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K020274Substantially Equivalent

Wmt Modular Ulnar Head Implant

Wrightmedicaltechnologyinc, Arlington TN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K020274 is the FDA 510(k) clearance record for WMT MODULAR ULNAR HEAD IMPLANT, a class II device, cleared for Wrightmedicaltechnologyinc on under FDA product code KXE (Prosthesis, Wrist, Hemi-, Ulnar). FDA records list 302 510(k) clearances for Wrightmedicaltechnologyinc, from to . As of , FDA records show no recalls naming K020274.

Clearance record

Decision date
Received
(25 days to decision)
Product code
KXE Prosthesis, Wrist, Hemi-, Ulnar
Regulation
21 CFR 888.3810
Device class
Class II
Review panel
Orthopedic
Applicant
Wrightmedicaltechnologyinc 5677 Airline Rd., Arlington TN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code KXE

Trailing 12 months

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

FDA records show no clearances under product code KXE in the twelve months to November 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KXE, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260
November 20260