Citrelock ACL Tibial Drill Guide 40-103-0009

GUDID 00810027270962

Acuitive Technologies, Inc.

Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable
Primary Device ID00810027270962
NIH Device Record Keyeebb308a-c74e-4cf6-8d1b-f145720ad2f3
Commercial Distribution StatusIn Commercial Distribution
Brand NameCitrelock ACL Tibial Drill Guide
Version Model Number40-103-0009
Catalog Number40-103-0009
Company DUNS074645634
Company NameAcuitive Technologies, 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 Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone201-661-2680
Emailmpoggie@acuitivetech.com
Phone201-661-2680
Emailmpoggie@acuitivetech.com
Phone201-661-2680
Emailmpoggie@acuitivetech.com
Phone201-661-2680
Emailmpoggie@acuitivetech.com
Phone201-661-2680
Emailmpoggie@acuitivetech.com
Phone201-661-2680
Emailmpoggie@acuitivetech.com
Phone201-661-2680
Emailmpoggie@acuitivetech.com
Phone201-661-2680
Emailmpoggie@acuitivetech.com
Phone201-661-2680
Emailmpoggie@acuitivetech.com
Phone201-661-2680
Emailmpoggie@acuitivetech.com
Phone201-661-2680
Emailmpoggie@acuitivetech.com
Phone201-661-2680
Emailmpoggie@acuitivetech.com
Phone201-661-2680
Emailmpoggie@acuitivetech.com
Phone201-661-2680
Emailmpoggie@acuitivetech.com
Phone201-661-2680
Emailmpoggie@acuitivetech.com
Phone201-661-2680
Emailmpoggie@acuitivetech.com
Phone201-661-2680
Emailmpoggie@acuitivetech.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100810027270962 [Primary]

FDA Product Code

HXYBrace, Drill

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00810027270962]

Moist Heat or Steam Sterilization

[00810027270962]

Moist Heat or Steam Sterilization

[00810027270962]

Moist Heat or Steam Sterilization

[00810027270962]

Moist Heat or Steam Sterilization

[00810027270962]

Moist Heat or Steam Sterilization

[00810027270962]

Moist Heat or Steam Sterilization

[00810027270962]

Moist Heat or Steam Sterilization

[00810027270962]

Moist Heat or Steam Sterilization

[00810027270962]

Moist Heat or Steam Sterilization

[00810027270962]

Moist Heat or Steam Sterilization

[00810027270962]

Moist Heat or Steam Sterilization

[00810027270962]

Moist Heat or Steam Sterilization

[00810027270962]

Moist Heat or Steam Sterilization

[00810027270962]

Moist Heat or Steam Sterilization

[00810027270962]

Moist Heat or Steam Sterilization

[00810027270962]

Moist Heat or Steam Sterilization

[00810027270962]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-07-03
Device Publish Date2023-06-23

Devices Manufactured by Acuitive Technologies, Inc.

00810027271471 - Citrelock ACL 1.1mm K-Wire2024-03-07
00810027270436 - Citrefix 2.9mm Inserter2023-07-03
00810027270443 - Citrefix 3.5mm Inserter2023-07-03
00810027270450 - Citrefix 4.5mm Inserter2023-07-03
00810027270467 - Citrefix 5.5mm Inserter2023-07-03
00810027270474 - Citrefix 2.9mm Drill2023-07-03
00810027270481 - Citrefix 3.5mm Drill2023-07-03
00810027270498 - Citrefix 4.5mm Drill2023-07-03
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.