510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K931107Substantially Equivalent

Logyk Acetabular Component System

Arthronics, Inc., Memphis TN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K931107 is the FDA 510(k) clearance record for LOGYK ACETABULAR COMPONENT SYSTEM, a class II device, cleared for Arthronics, Inc. on under FDA product code MBL (Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous). FDA records list 2 510(k) clearances for Arthronics, Inc., from to . As of , FDA records show no recalls naming K931107.

Clearance record

Decision date
Received
(390 days to decision)
Product code
MBL Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous
Regulation
21 CFR 888.3358
Device class
Class II
Review panel
Orthopedic
Applicant
Arthronics, Inc. 6685 Quince, Memphis TN
510(k) summary
Summary
Third party review
No

Clearances, product code MBL

Trailing 12 months

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

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