510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K203100Substantially Equivalent

Arthrex Eclipse Titanium Humeral Head

Arthrex GmbH, Naples FL / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K203100 is the FDA 510(k) clearance record for Arthrex Eclipse Titanium Humeral Head, a class II device, cleared for Arthrex, Inc. on under FDA product code PKC (Prosthesis, Total Anatomic Shoulder, Uncemented Metaphyseal Humeral Stem With No Diaphyseal Incursion, Semi-Constrained). FDA's definition for product code PKC reads: "Replacement of the humeral head for total anatomic shoulder arthroplasty". FDA records list 352 510(k) clearances for Arthrex, Inc., from to . As of , FDA records show no recalls naming K203100.

Clearance record

Decision date
Received
(37 days to decision)
Product code
PKC Prosthesis, Total Anatomic Shoulder, Uncemented Metaphyseal Humeral Stem With No Diaphyseal Incursion, Semi-Constrained
Regulation
21 CFR 888.3660
Device class
Class II
Review panel
Orthopedic
Applicant
Arthrex, Inc. 1370 Creekside Blvd., Naples FL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code PKC

Trailing 12 months
2 clearances under product code PKC in the twelve months to October 2026, May 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code PKC, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20261
June 20260
July 20260
August 20260
September 20261
October 20260