Implant Selection Device ISD-001

GUDID 10855068008331

Reusable surgical measurement instrument used when determining the size of the CurvaFix IM Implant to be used in a pelvic fixation procedure.

Curvafix Inc

Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable
Primary Device ID10855068008331
NIH Device Record Key829588ec-15a1-4c79-bd68-021c339d20f8
Commercial Distribution StatusIn Commercial Distribution
Brand NameImplant Selection Device
Version Model NumberISD-001
Catalog NumberISD-001
Company DUNS039779098
Company NameCurvafix Inc
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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 Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone425-276-8800
Emailsupport@curvafix.com
Phone425-276-8800
Emailsupport@curvafix.com
Phone425-276-8800
Emailsupport@curvafix.com
Phone425-276-8800
Emailsupport@curvafix.com
Phone425-276-8800
Emailsupport@curvafix.com
Phone425-276-8800
Emailsupport@curvafix.com
Phone425-276-8800
Emailsupport@curvafix.com
Phone425-276-8800
Emailsupport@curvafix.com
Phone425-276-8800
Emailsupport@curvafix.com
Phone425-276-8800
Emailsupport@curvafix.com
Phone425-276-8800
Emailsupport@curvafix.com
Phone425-276-8800
Emailsupport@curvafix.com
Phone425-276-8800
Emailsupport@curvafix.com
Phone425-276-8800
Emailsupport@curvafix.com
Phone425-276-8800
Emailsupport@curvafix.com
Phone425-276-8800
Emailsupport@curvafix.com
Phone425-276-8800
Emailsupport@curvafix.com
Phone425-276-8800
Emailsupport@curvafix.com
Phone425-276-8800
Emailsupport@curvafix.com
Phone425-276-8800
Emailsupport@curvafix.com
Phone425-276-8800
Emailsupport@curvafix.com
Phone425-276-8800
Emailsupport@curvafix.com
Phone425-276-8800
Emailsupport@curvafix.com
Phone425-276-8800
Emailsupport@curvafix.com
Phone425-276-8800
Emailsupport@curvafix.com
Phone425-276-8800
Emailsupport@curvafix.com
Phone425-276-8800
Emailsupport@curvafix.com
Phone425-276-8800
Emailsupport@curvafix.com
Phone425-276-8800
Emailsupport@curvafix.com
Phone425-276-8800
Emailsupport@curvafix.com
Phone425-276-8800
Emailsupport@curvafix.com
Phone425-276-8800
Emailsupport@curvafix.com
Phone425-276-8800
Emailsupport@curvafix.com

Device Identifiers

Device Issuing AgencyDevice ID
GS110855068008331 [Primary]

FDA Product Code

HWCScrew, Fixation, Bone

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10855068008331]

Moist Heat or Steam Sterilization

[10855068008331]

Moist Heat or Steam Sterilization

[10855068008331]

Moist Heat or Steam Sterilization

[10855068008331]

Moist Heat or Steam Sterilization

[10855068008331]

Moist Heat or Steam Sterilization

[10855068008331]

Moist Heat or Steam Sterilization

[10855068008331]

Moist Heat or Steam Sterilization

[10855068008331]

Moist Heat or Steam Sterilization

[10855068008331]

Moist Heat or Steam Sterilization

[10855068008331]

Moist Heat or Steam Sterilization

[10855068008331]

Moist Heat or Steam Sterilization

[10855068008331]

Moist Heat or Steam Sterilization

[10855068008331]

Moist Heat or Steam Sterilization

[10855068008331]

Moist Heat or Steam Sterilization

[10855068008331]

Moist Heat or Steam Sterilization

[10855068008331]

Moist Heat or Steam Sterilization

[10855068008331]

Moist Heat or Steam Sterilization

[10855068008331]

Moist Heat or Steam Sterilization

[10855068008331]

Moist Heat or Steam Sterilization

[10855068008331]

Moist Heat or Steam Sterilization

[10855068008331]

Moist Heat or Steam Sterilization

[10855068008331]

Moist Heat or Steam Sterilization

[10855068008331]

Moist Heat or Steam Sterilization

[10855068008331]

Moist Heat or Steam Sterilization

[10855068008331]

Moist Heat or Steam Sterilization

[10855068008331]

Moist Heat or Steam Sterilization

[10855068008331]

Moist Heat or Steam Sterilization

[10855068008331]

Moist Heat or Steam Sterilization

[10855068008331]

Moist Heat or Steam Sterilization

[10855068008331]

Moist Heat or Steam Sterilization

[10855068008331]

Moist Heat or Steam Sterilization

[10855068008331]

Moist Heat or Steam Sterilization

[10855068008331]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-12-10
Device Publish Date2021-12-02

On-Brand Devices [Implant Selection Device]

10855068008331Reusable surgical measurement instrument used when determining the size of the CurvaFix IM Impla
10855068008607Reusable surgical measurement instrument used when determining the size of the CurvaFix IM Impla
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