Atlas FDA

Ignite Stemless Anatomic Shoulder System

FDA 510(k) clearance K203108 · decided 2021-07-16

Clearance details

K-number
K203108
Device name
Ignite Stemless Anatomic Shoulder System
Applicant
Ignite Orthopedics, LLC
Decision
Substantially Equivalent
Date received
2020-10-15
Decision date
2021-07-16
Days to decision
274 days
Clearance type
Traditional
Product code
PKC
Device class
2
Regulation number
888.3660
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Winona Lake, IN, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

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
Easytech® Anatomical Shoulder System (K201391)Fx Shoulder USA, Inc.2021-02-16
Arthrex Eclipse Titanium Humeral Head (K203100)Arthrex, Inc.2020-11-20
Arthrex Eclipse Shoulder Prosthesis System (K201542)Arthrex, Inc.2020-07-08

Recalls involving this device

No recalls on record reference this clearance.