390-0220

GUDID 00886385022314

Sigmoid Notch Screw

Stryker Trauma SA

Wrist ulna-head prosthesis Wrist ulna-head prosthesis
Primary Device ID00886385022314
NIH Device Record Keya56955c1-53e0-4d88-8196-adec30b3467a
Commercial Distribution StatusIn Commercial Distribution
Version Model Number390-0220
Catalog Number390-0220
Company DUNS481999654
Company NameStryker Trauma SA
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 Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Length22 Millimeter
Length22 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100886385022314 [Primary]

FDA Product Code

KXEPROSTHESIS, WRIST, HEMI-, ULNAR

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2015-09-24

Devices Manufactured by Stryker Trauma SA

07613327414592 - PANGEA2024-03-11 Locking Screw
07613327414608 - PANGEA2024-03-11 Locking Screw
07613327414677 - PANGEA2024-03-11 Locking Screw
07613327414929 - PANGEA2024-03-11 Locking Screw
07613327415124 - PANGEA2024-03-11 Locking Screw
07613327415308 - PANGEA2024-03-11 Locking Screw
07613327415407 - PANGEA2024-03-11 Locking Screw
07613327415636 - PANGEA2024-03-11 Locking Screw

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