FDA.reportPublic FDA data

Arthrex®

Primary DI
00888867136151
Brand
Arthrex®
Company
ARTHREX, INC.
Model
AR-9148-18
Catalog number
AR-9148-18
Device description
HUMERAL HEAD 48/18
Published
2017-02-15
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
KWSPROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KWSProsthesis, Shoulder, Semi-Constrained, Metal/Polymer CementedOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K010124000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K010124000ARTHREX UNIVERS 30 SHOULDER PROSTHESISArthrex, Inc.2001-04-06KWS

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00888867136151PrimaryGS10
M150AR9148180SecondaryHIBCC0

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00888867136151008888671361518888671361510888867136151

GMDN Terms#

Term, Definition table
TermDefinition
Uncoated shoulder humeral stem prosthesisA sterile implantable device designed to provide fixation within the proximal humerus and a site of attachment for a humeral head or humeral body prosthesis as part of a shoulder joint replacement. The device is made of metal [e.g., titanium (Ti), cobalt-chrome (Co-Cr), stainless steel] and is not coated with a material intended to improve fixation and stability by promoting bone ingrowth. Fixation devices for implantation (e.g., screws) may be included and implantation is intended to be performed with bone cement.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+1(800)934-4404complaints@arthrex.com

Regulatory Flags#

DUNS number
131747628
Device count
1
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00888867020498Arthrex®AR-1648AR-16482018-08-03
00888867319882Arthrex®AR-8980BCTAR-8980BCT2021-06-24
00888867501317Arthrex®AR-1588SBR-RTTAR-1588SBR-RTT2025-06-23
00888867328693Arthrex®AR-8933VCL-10SAR-8933VCL-10S2024-08-05
00888867328709Arthrex®AR-8933VCL-12SAR-8933VCL-12S2024-08-05
00888867328716Arthrex®AR-8933VCL-14SAR-8933VCL-14S2024-08-05
00888867328723Arthrex®AR-8933VCL-16SAR-8933VCL-16S2024-08-05
00888867328730Arthrex®AR-8933VCL-18SAR-8933VCL-18S2024-08-05
00888867328747Arthrex®AR-8933VCL-20SAR-8933VCL-20S2024-08-05
00888867328754Arthrex®AR-8933VCL-22SAR-8933VCL-22S2024-08-05
00888867328761Arthrex®AR-8933VCL-24SAR-8933VCL-24S2024-08-05
00888867328778Arthrex®AR-8933VCL-26SAR-8933VCL-26S2024-08-05
00888867328785Arthrex®AR-8933VCL-28SAR-8933VCL-28S2024-08-05
00888867328792Arthrex®AR-8933VCL-30SAR-8933VCL-30S2024-08-05
00888867328808Arthrex®AR-8933VCL-32SAR-8933VCL-32S2024-08-05
00888867328815Arthrex®AR-8933VCL-34SAR-8933VCL-34S2024-08-05
00888867328822Arthrex®AR-8933VCL-36SAR-8933VCL-36S2024-08-05
00888867328839Arthrex®AR-8933VCL-38SAR-8933VCL-38S2024-08-05
00888867328846Arthrex®AR-8933VCL-40SAR-8933VCL-40S2024-08-05
00888867328860Arthrex®AR-8933HVCL-12SAR-8933HVCL-12S2024-08-05

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