510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K111145Substantially Equivalent

Endo Head

Medacta International SA, Camarillo CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K111145 is the FDA 510(k) clearance record for ENDO HEAD, a class II device, cleared for Medacta International on under FDA product code LZY (Prosthesis, Hip, Hemi-, Femoral, Metal Ball). FDA records list 205 510(k) clearances for Medacta International, from to . As of , FDA records show no recalls naming K111145.

Clearance record

Decision date
Received
(116 days to decision)
Product code
LZY Prosthesis, Hip, Hemi-, Femoral, Metal Ball
Regulation
21 CFR 888.3360
Device class
Class II
Review panel
Orthopedic
Applicant
Medacta International 4725 Calle Quetzal Unit B, Camarillo CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LZY

Trailing 12 months

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

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