Primary Device ID | 03700780601370 |
NIH Device Record Key | 6864c5c0-d8cb-4404-917f-80a048748895 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | KATIA™ |
Version Model Number | 60614016 |
Catalog Number | 60614016 |
Company DUNS | 296568400 |
Company Name | CLARIANCE |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 7738687041 |
s.chambat@clariance-spine.us | |
Phone | 7738687041 |
s.chambat@clariance-spine.us | |
Phone | 7738687041 |
s.chambat@clariance-spine.us | |
Phone | 7738687041 |
s.chambat@clariance-spine.us | |
Phone | 7738687041 |
s.chambat@clariance-spine.us | |
Phone | 7738687041 |
s.chambat@clariance-spine.us | |
Phone | 7738687041 |
s.chambat@clariance-spine.us | |
Phone | 7738687041 |
s.chambat@clariance-spine.us | |
Phone | 7738687041 |
s.chambat@clariance-spine.us | |
Phone | 7738687041 |
s.chambat@clariance-spine.us | |
Phone | 7738687041 |
s.chambat@clariance-spine.us | |
Phone | 7738687041 |
s.chambat@clariance-spine.us | |
Phone | 7738687041 |
s.chambat@clariance-spine.us |
Length | 16 Millimeter |
Outer Diameter | 4 Millimeter |
Length | 16 Millimeter |
Outer Diameter | 4 Millimeter |
Length | 16 Millimeter |
Outer Diameter | 4 Millimeter |
Length | 16 Millimeter |
Outer Diameter | 4 Millimeter |
Length | 16 Millimeter |
Outer Diameter | 4 Millimeter |
Length | 16 Millimeter |
Outer Diameter | 4 Millimeter |
Length | 16 Millimeter |
Outer Diameter | 4 Millimeter |
Length | 16 Millimeter |
Outer Diameter | 4 Millimeter |
Length | 16 Millimeter |
Outer Diameter | 4 Millimeter |
Length | 16 Millimeter |
Outer Diameter | 4 Millimeter |
Length | 16 Millimeter |
Outer Diameter | 4 Millimeter |
Length | 16 Millimeter |
Outer Diameter | 4 Millimeter |
Length | 16 Millimeter |
Outer Diameter | 4 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03700780601370 [Primary] |
ODP | Intervertebral Fusion Device With Bone Graft, Cervical |
Steralize Prior To Use | true |
Device Is Sterile | false |
[03700780601370]
Moist Heat or Steam Sterilization
[03700780601370]
Moist Heat or Steam Sterilization
[03700780601370]
Moist Heat or Steam Sterilization
[03700780601370]
Moist Heat or Steam Sterilization
[03700780601370]
Moist Heat or Steam Sterilization
[03700780601370]
Moist Heat or Steam Sterilization
[03700780601370]
Moist Heat or Steam Sterilization
[03700780601370]
Moist Heat or Steam Sterilization
[03700780601370]
Moist Heat or Steam Sterilization
[03700780601370]
Moist Heat or Steam Sterilization
[03700780601370]
Moist Heat or Steam Sterilization
[03700780601370]
Moist Heat or Steam Sterilization
[03700780601370]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2023-09-18 |
Device Publish Date | 2015-10-22 |
03700780622719 | ANTERIOR CERVICAL PLATE 1 LEVEL |
03700780622702 | ANTERIOR CERVICAL PLATE 1 LEVEL |
03700780622696 | ANTERIOR CERVICAL PLATE 1 LEVEL |
03700780622689 | ANTERIOR CERVICAL PLATE 1 LEVEL |
03700780622672 | ANTERIOR CERVICAL PLATE 1 LEVEL |
03700780622665 | ANTERIOR CERVICAL PLATE 1 LEVEL |
03700780616084 | ANTERIOR CERVICAL PLATE 1 LEVEL |
03700780601523 | SELF-TAPPING CANCELLOUS BONE SCREW - VARIABLE ANGLE |
03700780601424 | SELF-TAPPING CANCELLOUS BONE SCREW - VARIABLE ANGLE |
03700780601417 | SELF-TAPPING CANCELLOUS BONE SCREW - VARIABLE ANGLE |
03700780601394 | SELF-TAPPING CANCELLOUS BONE SCREW - VARIABLE ANGLE |
03700780601387 | SELF-TAPPING CANCELLOUS BONE SCREW - VARIABLE ANGLE |
03700780601370 | SELF-TAPPING CANCELLOUS BONE SCREW - VARIABLE ANGLE |
03700780601356 | SELF-TAPPING CANCELLOUS BONE SCREW - VARIABLE ANGLE |
03700780601349 | SELF-TAPPING CANCELLOUS BONE SCREW - VARIABLE ANGLE |
03700780601332 | SELF-TAPPING CANCELLOUS BONE SCREW - VARIABLE ANGLE |
03700780601325 | SELF-TAPPING CANCELLOUS BONE SCREW - VARIABLE ANGLE |
03700780601301 | SELF-TAPPING CANCELLOUS BONE SCREW - VARIABLE ANGLE |
03700780601295 | SELF-TAPPING CANCELLOUS BONE SCREW - VARIABLE ANGLE |
03700780601288 | SELF-DRILLING CANCELLOUS BONE SCREW - VARIABLE ANGLE |
03700780601271 | SELF-DRILLING CANCELLOUS BONE SCREW - VARIABLE ANGLE |
03700780601264 | SELF-DRILLING CANCELLOUS BONE SCREW - VARIABLE ANGLE |
03700780601257 | SELF-DRILLING CANCELLOUS BONE SCREW - VARIABLE ANGLE |
03700780601240 | SELF-DRILLING CANCELLOUS BONE SCREW - VARIABLE ANGLE |
03700780601233 | SELF-DRILLING CANCELLOUS BONE SCREW - VARIABLE ANGLE |
03700780601226 | SELF-DRILLING CANCELLOUS BONE SCREW - VARIABLE ANGLE |
03700780601219 | SELF-DRILLING CANCELLOUS BONE SCREW - VARIABLE ANGLE |
03700780601202 | SELF-DRILLING CANCELLOUS BONE SCREW - VARIABLE ANGLE |
03700780601066 | SELF-DRILLING CANCELLOUS BONE SCREW - VARIABLE ANGLE |
03700780601059 | SELF-DRILLING CANCELLOUS BONE SCREW - VARIABLE ANGLE |
03700780601042 | SELF-DRILLING CANCELLOUS BONE SCREW - VARIABLE ANGLE |
03700780601035 | SELF-TAPPING CANCELLOUS BONE SCREW - FIXED ANGLE |
03700780601028 | SELF-TAPPING CANCELLOUS BONE SCREW - FIXED ANGLE |
03700780601011 | SELF-TAPPING CANCELLOUS BONE SCREW - FIXED ANGLE |
03700780601004 | SELF-TAPPING CANCELLOUS BONE SCREW - FIXED ANGLE |
03700780600991 | SELF-TAPPING CANCELLOUS BONE SCREW - FIXED ANGLE |
03700780600984 | SELF-TAPPING CANCELLOUS BONE SCREW - FIXED ANGLE |
03700780600977 | SELF-TAPPING CANCELLOUS BONE SCREW - FIXED ANGLE |
03700780600960 | SELF-TAPPING CANCELLOUS BONE SCREW - FIXED ANGLE |
03700780600953 | SELF-TAPPING CANCELLOUS BONE SCREW - FIXED ANGLE |
03700780600946 | SELF-TAPPING CANCELLOUS BONE SCREW - FIXED ANGLE |
03700780600939 | SELF-TAPPING CANCELLOUS BONE SCREW - FIXED ANGLE |
03700780600915 | SELF-TAPPING CANCELLOUS BONE SCREW - FIXED ANGLE |
03700780600908 | ANTERIOR CERVICAL PLATE 5 LEVELS |
03700780600892 | ANTERIOR CERVICAL PLATE 5 LEVELS |
03700780600885 | ANTERIOR CERVICAL PLATE 5 LEVELS |
03700780600878 | ANTERIOR CERVICAL PLATE 5 LEVELS |
03700780600861 | ANTERIOR CERVICAL PLATE 5 LEVELS |
03700780600854 | ANTERIOR CERVICAL PLATE 5 LEVELS |
03700780600830 | ANTERIOR CERVICAL PLATE 4 LEVELS |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
KATIA 88412985 not registered Live/Pending |
Smirnov, Katrina 2019-05-02 |
KATIA 88337814 not registered Dead/Abandoned |
Al Madar United Trading Company 2019-03-13 |
KATIA 87183498 not registered Dead/Abandoned |
AS IP Holdco, LLC 2016-09-26 |
KATIA 86934141 5063526 Live/Registered |
Luo Lin 2016-03-09 |
KATIA 86573569 not registered Dead/Abandoned |
Katia Fashion, Inc. 2015-03-23 |
KATIA 79129185 4508634 Live/Registered |
katia SA 2013-02-18 |
KATIA 78667667 not registered Dead/Abandoned |
MGA Entertainment, Inc. 2005-07-11 |
KATIA 78293955 not registered Dead/Abandoned |
Cyberscan Technology 2003-08-29 |
KATIA 76486181 3094602 Dead/Cancelled |
Chestnuts LLC 2003-01-30 |
KATIA 76417271 2717346 Live/Registered |
Fil Katia, S.A. 2002-06-03 |
KATIA 75803746 2417271 Dead/Cancelled |
Gordeeva, Ekaterina 1999-09-17 |
KATIA 75362165 not registered Dead/Abandoned |
Gordeeva, Ekaterina 1997-09-24 |