PROPHECY INFINITY 33600200

GUDID 00889797004879

WRIGHT MEDICAL TECHNOLOGY, INC.

Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable Orthopaedic implant aiming/guiding block, reusable
Primary Device ID00889797004879
NIH Device Record Keya4089fb9-4fec-4b7c-95f6-619edba547d2
Commercial Distribution StatusIn Commercial Distribution
Brand NamePROPHECY INFINITY
Version Model Number33600200
Catalog Number33600200
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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100889797004879 [Primary]

FDA Product Code

HSNPROSTHESIS, ANKLE, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00889797004879]

Moist Heat or Steam Sterilization


[00889797004879]

Moist Heat or Steam Sterilization


[00889797004879]

Moist Heat or Steam Sterilization


[00889797004879]

Moist Heat or Steam Sterilization


[00889797004879]

Moist Heat or Steam Sterilization


[00889797004879]

Moist Heat or Steam Sterilization


[00889797004879]

Moist Heat or Steam Sterilization


[00889797004879]

Moist Heat or Steam Sterilization


[00889797004879]

Moist Heat or Steam Sterilization


[00889797004879]

Moist Heat or Steam Sterilization


[00889797004879]

Moist Heat or Steam Sterilization


[00889797004879]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2022-05-16
Device Publish Date2016-09-17

On-Brand Devices [PROPHECY INFINITY]

00889797057134PROPINF
0088979700487933600200
00889797103374Tibial Resection Guide Insert
00889797102438Reversible Talar Resection Guide
00889797102421Tibial Corner Protector Peg
00889797102414Tibial Resection Guide Insert
00889797102407Tibial Resection Guide Insert
00889797102391Tibial Resection Guide Insert

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