FDA.reportPublic FDA data

Paragon

Primary DI
09340499024707
Brand
Paragon
Company
GLOBAL MANUFACTURING TECHNOLOGY PTY LIMITED
Model
GM08001-322-06
Catalog number
GM08001-322-06
Device description
Paragon Trial Neck High Offset Size 7 - 9 - Female (Omni)
Published
2016-09-09
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
LZOProsthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
MEHProsthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
LZOProsthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, UncementedOrthopedic2
MEHProsthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium PhosphateOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K123782000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K123782000PARAGON HIP SYSTEMGlobal Manufacturing Technology2013-03-14LZO

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
09340499024707PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
09340499024707093404990247079340499024707

GMDN Terms#

Term, Definition table
TermDefinition
Femoral stem prosthesis trialA copy of a final femoral stem prosthesis designed to be used for trial reductions during hip arthroplasty to judge the correct offset, leg-length, and range of motion of the final femoral prosthesis to be implanted. It is one of a set, or a set, of graduated sizes, and is used in conjunction with femoral head trial prostheses. It is typically made of metal or polymer material and includes trial stems, trial sleeves, and trial necks. This is a reusable device intended to be sterilized prior to use.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Device Size Text, specify0

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+6128870100info@globalortho.com.au

Regulatory Flags#

DUNS number
752039982
Device count
1
Lot or batch
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
09340499024509ParagonGM08001-311-00GM08001-311-002016-09-09
09340499005195GRU TibiaGRU-0T-6.5-P-RGRU-0T-6.5-P-R2016-03-21
09340499005201GRU TibiaGRU-0T-7.5-P-RGRU-0T-7.5-P-R2016-03-23
09340499005218GRU TibiaGRU-0T-8.5-P-RGRU-0T-8.5-P-R2016-03-23
09340499005225GRU TibiaGRU-0T-9.5-P-RGRU-0T-9.5-P-R2016-03-23
09340499005232GRU TibiaGRU-1T-6.5-P-RGRU-1T-6.5-P-R2016-03-23
09340499005249GRU TibiaGRU-1T-7.5-P-RGRU-1T-7.5-P-R2016-03-23
09340499005256GRU TibiaGRU-1T-8.5-P-RGRU-1T-8.5-P-R2016-03-23
09340499005263GRU TibiaGRU-1T-9.5-P-RGRU-1T-9.5-P-R2016-03-23
09340499005270GRU TibiaGRU-2T-6.5-P-RGRU-2T-6.5-P-R2016-03-23
09340499005287GRU TibiaGRU-2T-7.5-P-RGRU-2T-7.5-P-R2016-03-23
09340499005294GRU TibiaGRU-2T-8.5-P-RGRU-2T-8.5-P-R2016-03-23
09340499005300GRU TibiaGRU-2T-9.5-P-RGRU-2T-9.5-P-R2016-03-23
09340499005317GRU TibiaGRU-3T-6.5-P-RGRU-3T-6.5-P-R2016-03-23
09340499005324GRU TibiaGRU-3T-7.5-P-RGRU-3T-7.5-P-R2016-03-23
09340499005331GRU TibiaGRU-3T-8.5-P-RGRU-3T-8.5-P-R2016-03-23
09340499005348GRU TibiaGRU-3T-9.5-P-RGRU-3T-9.5-P-R2016-03-23
09340499005355GRU TibiaGRU-4T-6.5-P-RGRU-4T-6.5-P-R2016-03-23
09340499005362GRU TibiaGRU-4T-7.5-P-RGRU-4T-7.5-P-R2016-03-23
09340499005379GRU TibiaGRU-4T-8.5-P-RGRU-4T-8.5-P-R2016-03-23

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00810030811992InSitu Hip SystemNEXTSTEP ARTHROPEDIX, LLCLZO2026-06-01
00810030812036InSitu Hip SystemNEXTSTEP ARTHROPEDIX, LLCLZO2026-06-01
00810030812043InSitu Hip SystemNEXTSTEP ARTHROPEDIX, LLCLZO2026-06-01
00810030812050InSitu Hip SystemNEXTSTEP ARTHROPEDIX, LLCLZO2026-06-01
00810030812067InSitu Hip SystemNEXTSTEP ARTHROPEDIX, LLCLZO2026-06-01
00810030812074InSitu Hip SystemNEXTSTEP ARTHROPEDIX, LLCLZO2026-06-01
00810030812081InSitu Hip SystemNEXTSTEP ARTHROPEDIX, LLCLZO2026-06-01
00810030812098InSitu Hip SystemNEXTSTEP ARTHROPEDIX, LLCLZO2026-06-01
00810030812104InSitu Hip SystemNEXTSTEP ARTHROPEDIX, LLCLZO2026-06-01
00810030812111InSitu Hip SystemNEXTSTEP ARTHROPEDIX, LLCLZO2026-06-01
00810030812128InSitu Hip SystemNEXTSTEP ARTHROPEDIX, LLCLZO2026-06-01
00810030812135InSitu Hip SystemNEXTSTEP ARTHROPEDIX, LLCLZO2026-06-01
00810030812142InSitu Hip SystemNEXTSTEP ARTHROPEDIX, LLCLZO2026-06-01
00810030812159InSitu Hip SystemNEXTSTEP ARTHROPEDIX, LLCLZO2026-06-01
00810030812173InSitu Hip SystemNEXTSTEP ARTHROPEDIX, LLCLZO2026-06-01
00810030812180InSitu Hip SystemNEXTSTEP ARTHROPEDIX, LLCLZO2026-06-01
00810030812197InSitu Hip SystemNEXTSTEP ARTHROPEDIX, LLCLZO2026-06-01
00810030812203InSitu Hip SystemNEXTSTEP ARTHROPEDIX, LLCLZO2026-06-01
00810030812210InSitu Hip SystemNEXTSTEP ARTHROPEDIX, LLCLZO2026-06-01
00810030812227InSitu Hip SystemNEXTSTEP ARTHROPEDIX, LLCLZO2026-06-01
00810030812234InSitu Hip SystemNEXTSTEP ARTHROPEDIX, LLCLZO2026-06-01
00810030812241InSitu Hip SystemNEXTSTEP ARTHROPEDIX, LLCLZO2026-06-01
00810030812258InSitu Hip SystemNEXTSTEP ARTHROPEDIX, LLCLZO2026-06-01
00810030812265InSitu Hip SystemNEXTSTEP ARTHROPEDIX, LLCLZO2026-06-01
00810030812272InSitu Hip SystemNEXTSTEP ARTHROPEDIX, LLCLZO2026-06-01
00810030812289InSitu Hip SystemNEXTSTEP ARTHROPEDIX, LLCLZO2026-06-01
00810030812296InSitu Hip SystemNEXTSTEP ARTHROPEDIX, LLCLZO2026-06-01
00810030812319InSitu Hip SystemNEXTSTEP ARTHROPEDIX, LLCLZO2026-06-01
00810030812326InSitu Hip SystemNEXTSTEP ARTHROPEDIX, LLCLZO2026-06-01
00810030812333InSitu Hip SystemNEXTSTEP ARTHROPEDIX, LLCLZO2026-06-01