SImmetry Implant, 8.5mm x 95mm

GUDID 04260636674433

Paradigm Spine GmbH

Sacroiliac joint transarticular fixation/arthrodesis implant, coated
Primary Device ID04260636674433
NIH Device Record Keyfc63c5e4-e017-476c-a787-5ac3c5123c84
Commercial Distribution StatusIn Commercial Distribution
Brand NameSImmetry Implant, 8.5mm x 95mm
Version Model Number10-S08595-01
Company DUNS537619731
Company NameParadigm Spine GmbH
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
GS104260636674433 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

OURSacroiliac Joint Fixation

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-02-02
Device Publish Date2021-01-25

Devices Manufactured by Paradigm Spine GmbH

04260636678998 - coflex instrument loaner set2023-04-10 instrument loaner set
04260636678912 - CoFix instrument loaner set2021-06-29
04260636678929 - CoFix implant loaner set2021-06-29
04260636673467 - SImmetry, Blunt Pin, 3.2mm2021-02-02
04260636673474 - SImmetry, Impactor2021-02-02
04260636673481 - SImmetry, Long Pin, 3.2mm2021-02-02
04260636673498 - SImmetry, Short Pin, 3.2mm2021-02-02
04260636673504 - SImmetry, Working Cannula2021-02-02

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