Atlas FDA

Arthrex Eclipse Titanium Humeral Head

FDA 510(k) clearance K203100 · decided 2020-11-20

Clearance details

K-number
K203100
Device name
Arthrex Eclipse Titanium Humeral Head
Applicant
Arthrex, Inc.
Decision
Substantially Equivalent
Date received
2020-10-14
Decision date
2020-11-20
Days to decision
37 days
Clearance type
Special
Product code
PKC
Device class
2
Regulation number
888.3660
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Naples, FL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

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RecordFirmDate
FX V135 EASYTECH® Shoulder System (K254154)FX Shoulder Solutions, Inc.2026-05-01
AETOS Shoulder System Stemless Humeral Prosthesis (K252129)Smith & Nephew, Inc.2025-10-03
INHANCE INTACT™ (K243248)Depuy Ireland UC2024-12-23
OsseoFit Stemless Shoulder System (K241873)Zimmer, Inc.2024-12-11
AETOS Shoulder System Stemless Humeral Prosthesis (K240716)Smith & Nephew, Inc.2024-11-20
SMR Stemless Anatomic (K221758)Lima Corporate S.P.A.2023-03-17
Tornier Perform Humeral System – Stemless (K220418)Tornier, Inc.2022-09-14
Shoulder Innovations Total Shoulder System (K213615)Shoulder Innovations, Inc.2022-03-11
GLOBAL ICON Stemless Shoulder System (K212683)Depuy(Ireland)2022-01-19
Ignite Stemless Anatomic Shoulder System (K203108)Ignite Orthopedics, LLC2021-07-16
Easytech® Anatomical Shoulder System (K201391)Fx Shoulder USA, Inc.2021-02-16
Arthrex Eclipse Shoulder Prosthesis System (K201542)Arthrex, Inc.2020-07-08

Recalls involving this device

No recalls on record reference this clearance.