Conventus Cage - DR, Large

GUDID 00814289020013

CONVENTUS ORTHOPAEDICS, INC.

Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile
Primary Device ID00814289020013
NIH Device Record Key0615fc78-043f-452b-b16d-14b410b2a86b
Commercial Distribution StatusIn Commercial Distribution
Brand NameConventus Cage - DR, Large
Version Model NumberDRS-L
Company DUNS021231299
Company NameCONVENTUS ORTHOPAEDICS, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
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 Identifiers

Device Issuing AgencyDevice ID
GS100814289020013 [Primary]

FDA Product Code

HSBRod, Fixation, Intramedullary And Accessories

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 Date2015-09-18

Devices Manufactured by CONVENTUS ORTHOPAEDICS, INC.

00814289020754 - Conventus Cage - PR, Small2018-07-06
00814289020761 - Conventus Cage - PR, Large2018-07-06
00814289020006 - Conventus Cage - DR, Small2018-03-29
00814289020013 - Conventus Cage - DR, Large2018-03-29
00814289020013 - Conventus Cage - DR, Large2018-03-29
00814289020020 - 2.7mm x 8mm Cannulated Headed Screw2018-03-29
00814289020037 - 2.7mm x 10mm Cannulated Headed Screw2018-03-29
00814289020044 - 2.7mm x 12mm Cannulated Headed Screw2018-03-29
00814289020051 - 2.7mm x 14mm Cannulated Headed Screw2018-03-29

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