CAROLINA JONES

GUDID 00840420134974

WRIGHT MEDICAL TECHNOLOGY, INC.

Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile
Primary Device ID00840420134974
NIH Device Record Keyb0ce13b8-58ac-459b-b0b0-e4cbcfa17b29
Commercial Distribution StatusIn Commercial Distribution
Brand NameCAROLINA JONES
Version Model Number56004540
Company DUNS807201207
Company NameWRIGHT MEDICAL TECHNOLOGY, INC.
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

Customer Support Contacts

Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com

Device Dimensions

Length40 Millimeter
Outer Diameter4.5 Millimeter
Device Size Text, specify0
Length40 Millimeter
Outer Diameter4.5 Millimeter
Device Size Text, specify0
Length40 Millimeter
Outer Diameter4.5 Millimeter
Device Size Text, specify0
Length40 Millimeter
Outer Diameter4.5 Millimeter
Device Size Text, specify0
Length40 Millimeter
Outer Diameter4.5 Millimeter
Device Size Text, specify0
Length40 Millimeter
Outer Diameter4.5 Millimeter
Device Size Text, specify0
Length40 Millimeter
Outer Diameter4.5 Millimeter
Device Size Text, specify0
Length40 Millimeter
Outer Diameter4.5 Millimeter
Device Size Text, specify0
Length40 Millimeter
Outer Diameter4.5 Millimeter
Device Size Text, specify0
Length40 Millimeter
Outer Diameter4.5 Millimeter
Device Size Text, specify0
Length40 Millimeter
Outer Diameter4.5 Millimeter
Device Size Text, specify0
Length40 Millimeter
Outer Diameter4.5 Millimeter
Device Size Text, specify0
Length40 Millimeter
Outer Diameter4.5 Millimeter
Device Size Text, specify0
Length40 Millimeter
Outer Diameter4.5 Millimeter
Device Size Text, specify0
Length40 Millimeter
Outer Diameter4.5 Millimeter
Device Size Text, specify0
Length40 Millimeter
Outer Diameter4.5 Millimeter
Device Size Text, specify0
Length40 Millimeter
Outer Diameter4.5 Millimeter
Device Size Text, specify0
Length40 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100840420134974 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HWCScrew, fixation, bone

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-10-15

On-Brand Devices [CAROLINA JONES]

0084042013501840112714
0084042013500156006565
0084042013499856005565
0084042013498156004565
0084042013497456004540
0084042013495040110015

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