FDA.reportPublic FDA data

SmartBase Central Pillar

Primary DI
00811813020303
Brand
SmartBase Central Pillar
Company
CUSTOM ORTHOPAEDIC SOLUTIONS, INC.
Model
K
Catalog number
0006-0033
Device description
The SmartBase Central Pillar is a component of the SmartBase that holds the guide pin to set the Intelligent Reusable Instrument (IRI) according to a patient-specific preoperative plan. The SmartBase Central Pillar is indicated for use as part of the Arthrex Glenoid Intelligent Reusable Instrument System (IRIS) in Total Shoulder Arthroplasty (TSA).
Published
2016-09-02
Public version status
Update
Distribution status
Not in Commercial Distribution
MRI safety
MR Unsafe
Rx
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
KWSProsthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented
PHXShoulder Prosthesis, Reverse Configuration

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KWSProsthesis, Shoulder, Semi-Constrained, Metal/Polymer CementedOrthopedic2
PHXShoulder Prosthesis, Reverse ConfigurationOrthopedic2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00811813020303PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00811813020303008118130203038118130203030811813020303

GMDN Terms#

Term, Definition table
TermDefinition
Orthopaedic bone pin holderA non-sterile cylindrical device intended to temporarily hold one or more orthopaedic pin(s) [e.g., K-wires] during sterilization and a surgical procedure for protection against damage. It is made of metal (e.g., stainless steel) and is typically a cylinder with a screw top, with lateral fenestartions to enable the penetration of sterilization fluid. This is a reusable device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Length38.1Millimeter
Lumen/Inner Diameter0.132Inch
Outer Diameter0.188Inch

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Special Storage Condition, Specify00Store in a dry, dark, cool place.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
2168005905info@customorthopaedics.com

Regulatory Flags#

DUNS number
078667390
Device count
1
Lot or batch
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00811813020525VisionAir 3D Stent0010-01262024-03-11
00811813020006Glenoid IRI HandleM0006-00012016-09-02
00811813020013Glenoid IRI BarrelM0006-00022016-09-02
00811813020020Glenoid IRIS Surgical TrayE0006-00112016-09-02
00811813020037Glenoid IRI CapJ0006-00032016-09-02
00811813020044Glenoid IRI Leg (10mm)L0006-0005-102016-09-02
00811813020051Glenoid IRI Leg (11mm)L0006-0005-112016-09-02
00811813020068Glenoid IRI Leg (12mm)L0006-0005-122016-09-02
00811813020075Glenoid IRI Leg (13mm)L0006-0005-132016-09-02
00811813020082Glenoid IRI Leg (14mm)L0006-0005-142016-09-02
00811813020099Glenoid IRI Leg (15mm)L0006-0005-152016-09-02
00811813020105Glenoid IRI Leg (16mm)L0006-0005-162016-09-02
00811813020112Glenoid IRI Leg (17mm)L0006-0005-172016-09-02
00811813020129Glenoid IRI Leg (18mm)L0006-0005-182016-09-02
00811813020136Glenoid IRI Leg (19mm)L0006-0005-192016-09-02
00811813020143Glenoid IRI Leg (20mm)L0006-0005-202016-09-02
00811813020150Glenoid IRI Leg (21mm)L0006-0005-212016-09-02
00811813020167Glenoid IRI Leg (22mm)L0006-0005-222016-09-02
00811813020174Glenoid IRI Leg (23mm)L0006-0005-232016-09-02
00811813020181Glenoid IRI Leg (24mm)L0006-0005-242016-09-02

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
03701037320440FX V135 Shoulder ProsthesisFX SOLUTIONSPHX2026-09-22
03701037321188ORTHOPEDIC MANUAL SURGICAL INSTRUMENTFX SOLUTIONSPHX2026-09-22
00840097533919Veritas HemiarthroplastyRestor3d, Inc.PHX2026-09-18
00840097533926Veritas HemiarthroplastyRestor3d, Inc.PHX2026-09-18
00840097533933Veritas HemiarthroplastyRestor3d, Inc.PHX2026-09-18
00840097533940Veritas HemiarthroplastyRestor3d, Inc.PHX2026-09-18
00840097533957Veritas HemiarthroplastyRestor3d, Inc.PHX2026-09-18
00840097533964Veritas HemiarthroplastyRestor3d, Inc.PHX2026-09-18
00840097533971Veritas HemiarthroplastyRestor3d, Inc.PHX2026-09-18
00840097533988Veritas HemiarthroplastyRestor3d, Inc.PHX2026-09-18
00840097533995Veritas HemiarthroplastyRestor3d, Inc.PHX2026-09-18
00840097534008Veritas HemiarthroplastyRestor3d, Inc.PHX2026-09-18
00840097534015Veritas HemiarthroplastyRestor3d, Inc.PHX2026-09-18
00840097534022Veritas HemiarthroplastyRestor3d, Inc.PHX2026-09-18
B1132N2GI200050Shoulder Innovations InSet GOShoulder Innovations, Inc.KWS2026-09-18
B1132N2GI200100Shoulder Innovations InSet GOShoulder Innovations, Inc.KWS2026-09-18
B1132N2GI206000Shoulder Innovations InSet GOShoulder Innovations, Inc.KWS2026-09-18
B1132N2GI208000Shoulder Innovations InSet GOShoulder Innovations, Inc.KWS2026-09-18
B1132N2GI220050Shoulder Innovations InSet GOShoulder Innovations, Inc.KWS2026-09-18
B1132N2GI220100Shoulder Innovations InSet GOShoulder Innovations, Inc.KWS2026-09-18
B1132N2GI226000Shoulder Innovations InSet GOShoulder Innovations, Inc.KWS2026-09-18
B1132N2GI228000Shoulder Innovations InSet GOShoulder Innovations, Inc.KWS2026-09-18
B1132N2GI240050Shoulder Innovations InSet GOShoulder Innovations, Inc.KWS2026-09-18
B1132N2GI240100Shoulder Innovations InSet GOShoulder Innovations, Inc.KWS2026-09-18
B1132N2GI246000Shoulder Innovations InSet GOShoulder Innovations, Inc.KWS2026-09-18
B1132N2GI248000Shoulder Innovations InSet GOShoulder Innovations, Inc.KWS2026-09-18
B1132N2GI270050Shoulder Innovations InSet GOShoulder Innovations, Inc.KWS2026-09-18
B1132N2GI270100Shoulder Innovations InSet GOShoulder Innovations, Inc.KWS2026-09-18
B1132N2GI276000Shoulder Innovations InSet GOShoulder Innovations, Inc.KWS2026-09-18
B1132N2GI278000Shoulder Innovations InSet GOShoulder Innovations, Inc.KWS2026-09-18