Rx Knee All Poly Tibia Augment - 3deg Wedge

GUDID 09348215124083

SIGNATURE ORTHOPAEDICS PTY LTD

Temporary knee prosthesis, non-customized
Primary Device ID09348215124083
NIH Device Record Keyd5ec4137-e266-4703-8bc6-e9a9677da98a
Commercial Distribution StatusIn Commercial Distribution
Brand NameRx Knee All Poly Tibia Augment - 3deg Wedge
Version Model Number121-20-9221
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS109348215124083 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JWHProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-11-20
Device Publish Date2024-11-12

On-Brand Devices [Rx Knee All Poly Tibia Augment - 3deg Wedge]

09348215124168121-20-9229
09348215124151121-20-9228
09348215124144121-20-9227
09348215124137121-20-9226
09348215124120121-20-9225
09348215124113121-20-9224
09348215124106121-20-9223
09348215124090121-20-9222
09348215124083121-20-9221
09348215124076121-20-9319
09348215124069121-20-9318
09348215124052121-20-9317
09348215124045121-20-9316
09348215124038121-20-9315
09348215124021121-20-9314
09348215124014121-20-9313
09348215124007121-20-9312
09348215123994121-20-9311
09348215111892121-20-9309
09348215111885121-20-9308
09348215111878121-20-9307
09348215111861121-20-9306
09348215111854121-20-9305
09348215111847121-20-9304
09348215111830121-20-9303
09348215111823121-20-9302
09348215111816121-20-9301
09348215110864121-20-9239
09348215110857121-20-9238
09348215110840121-20-9237
09348215110833121-20-9236
09348215110826121-20-9235
09348215110819121-20-9234
09348215110802121-20-9233
09348215110796121-20-9232
09348215110789121-20-9231

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