World Stem Trial Size 8M

GUDID 09348215064822

SIGNATURE ORTHOPAEDICS PTY LTD

Surgical implant template, reusable
Primary Device ID09348215064822
NIH Device Record Keyf6ff553e-2978-474f-9b41-c0a931392d0a
Commercial Distribution StatusIn Commercial Distribution
Brand NameWorld Stem Trial Size 8M
Version Model Number112-42-2821
Company DUNS751993028
Company NameSIGNATURE ORTHOPAEDICS PTY LTD
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS109348215064822 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MEHProsthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[09348215064822]

Moist Heat or Steam Sterilization


[09348215064822]

Moist Heat or Steam Sterilization


[09348215064822]

Moist Heat or Steam Sterilization


[09348215064822]

Moist Heat or Steam Sterilization


[09348215064822]

Moist Heat or Steam Sterilization


[09348215064822]

Moist Heat or Steam Sterilization


[09348215064822]

Moist Heat or Steam Sterilization


[09348215064822]

Moist Heat or Steam Sterilization


[09348215064822]

Moist Heat or Steam Sterilization


[09348215064822]

Moist Heat or Steam Sterilization


[09348215064822]

Moist Heat or Steam Sterilization


[09348215064822]

Moist Heat or Steam Sterilization


[09348215064822]

Moist Heat or Steam Sterilization


[09348215064822]

Moist Heat or Steam Sterilization


[09348215064822]

Moist Heat or Steam Sterilization


[09348215064822]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-05-17
Device Publish Date2021-05-07

Devices Manufactured by SIGNATURE ORTHOPAEDICS PTY LTD

09348215110246 - Rx Knee All Poly Tibia Augment - Full - 4mm2024-11-20
09348215110253 - Rx Knee All Poly Tibia Augment - Full - 4mm2024-11-20
09348215110260 - Rx Knee All Poly Tibia Augment - Full - 4mm2024-11-20
09348215110277 - Rx Knee All Poly Tibia Augment - Full - 4mm2024-11-20
09348215110284 - Rx Knee All Poly Tibia Augment - Full - 4mm2024-11-20
09348215110291 - Rx Knee All Poly Tibia Augment - Full - 4mm2024-11-20
09348215110307 - Rx Knee All Poly Tibia Augment - Full - 4mm2024-11-20
09348215110314 - Rx Knee All Poly Tibia Augment - Full - 4mm2024-11-20

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.