ORTHOLOC 3Di CROSSCHECK

GUDID 00840420187819

WRIGHT MEDICAL TECHNOLOGY, INC.

Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile
Primary Device ID00840420187819
NIH Device Record Key0b17484b-2fd1-478a-bd16-209e7066adce
Commercial Distribution StatusIn Commercial Distribution
Brand NameORTHOLOC 3Di CROSSCHECK
Version Model Number582SX3520
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

Device Dimensions

Outer Diameter3.5 Millimeter
Length20 Millimeter
Device Size Text, specify0
Outer Diameter3.5 Millimeter
Length20 Millimeter
Device Size Text, specify0
Outer Diameter3.5 Millimeter
Length20 Millimeter
Device Size Text, specify0
Outer Diameter3.5 Millimeter
Length20 Millimeter
Device Size Text, specify0
Outer Diameter3.5 Millimeter
Length20 Millimeter
Device Size Text, specify0
Outer Diameter3.5 Millimeter
Length20 Millimeter
Device Size Text, specify0
Outer Diameter3.5 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100840420187819 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HRSPlate, 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 Date2016-09-17

On-Brand Devices [ORTHOLOC 3Di CROSSCHECK]

008897970408605820CX25
00840420187918582SX3540
00840420187901582SX3538
00840420187895582SX3536
00840420187888582SX3534
00840420187871582SX3532
00840420187864582SX3530
00840420187857582SX3528
00840420187840582SX3526
00840420187833582SX3524
00840420187826582SX3522
00840420187819582SX3520
00840420187802582SX3518
00840420187796582SYPX1
00840420187765582SUTN5
00840420187727582SMPX1R
00840420187710582SMPX1L
00840420187703582SLPX2R
00840420187697582SLPX2L
00840420187680582SLPX0R
00840420187673582SLPX0L

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