Dakota ALIF Plate System 69-AL-1519

GUDID 00840019962186

36X 28 X 19mm X 15° PEEK

PRECISION SPINE, INC.

Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage
Primary Device ID00840019962186
NIH Device Record Keybed268e8-9822-4273-bcb8-d3b254aff2d5
Commercial Distribution StatusIn Commercial Distribution
Brand NameDakota ALIF Plate System
Version Model Number69-AL-1519
Catalog Number69-AL-1519
Company DUNS079398589
Company NamePRECISION SPINE, INC.
Device Count1
DM Exempttrue
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 Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100840019962186 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KWQAppliance, Fixation, Spinal Intervertebral Body
OVDIntervertebral Fusion Device With Integrated Fixation, Lumbar

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00840019962186]

Moist Heat or Steam Sterilization


[00840019962186]

Moist Heat or Steam Sterilization


[00840019962186]

Moist Heat or Steam Sterilization


[00840019962186]

Moist Heat or Steam Sterilization


[00840019962186]

Moist Heat or Steam Sterilization


[00840019962186]

Moist Heat or Steam Sterilization


[00840019962186]

Moist Heat or Steam Sterilization


[00840019962186]

Moist Heat or Steam Sterilization


[00840019962186]

Moist Heat or Steam Sterilization


[00840019962186]

Moist Heat or Steam Sterilization


[00840019962186]

Moist Heat or Steam Sterilization


[00840019962186]

Moist Heat or Steam Sterilization


[00840019962186]

Moist Heat or Steam Sterilization


[00840019962186]

Moist Heat or Steam Sterilization


[00840019962186]

Moist Heat or Steam Sterilization


[00840019962186]

Moist Heat or Steam Sterilization


[00840019962186]

Moist Heat or Steam Sterilization


[00840019962186]

Moist Heat or Steam Sterilization


[00840019962186]

Moist Heat or Steam Sterilization


[00840019962186]

Moist Heat or Steam Sterilization


[00840019962186]

Moist Heat or Steam Sterilization


[00840019962186]

Moist Heat or Steam Sterilization


[00840019962186]

Moist Heat or Steam Sterilization


[00840019962186]

Moist Heat or Steam Sterilization


[00840019962186]

Moist Heat or Steam Sterilization


[00840019962186]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-01-31
Device Publish Date2022-01-21

On-Brand Devices [Dakota ALIF Plate System]

0084001996170730X 26 X 19mm X 15° PEEK
0084001996169130X 26 X 17mm X 15° PEEK
0084001996168430X 26 X 15mm X 15° PEEK
0084001996167730X 26 X 13mm X 15° PEEK
0084001996166030X 26 X 11mm X 15° PEEK
0084001996165330X 26 X 19mm X 8° PEEK
0084001996164630X 26 X 17mm X 8° PEEK
0084001996163930X 26 X 15mm X 8° PEEK
0084001996162230X 26 X 13mm X 8° PEEK
0084001996161530X 26 X 11mm X 8° PEEK
0084001996160830 X 26 X 19mm X 0° PEEK
0084001996159230 X 26 X 17mm X 0° PEEK
0084001996158530 X 26 X 15mm X 0° PEEK
0084001996157830 X 26 X 13mm X 0° PEEK
0084001996156130 X 26 X 11mm X 0° PEEK
0084001996200133X 27 X 17mm X 25° PEEK
0084001996199833X 27 X 15mm X 25° PEEK
0084001996198133X 27 X 19mm X 20° PEEK
0084001996197433X 27 X 17mm X 20° PEEK
0084001996196733X 27 X 15mm X 20° PEEK
0084001996195033X 27 X 13mm X 20° PEEK
0084001996194333X 27 X 19mm X 15° PEEK
0084001996193633X 27 X 17mm X 15° PEEK
0084001996192933X 27 X 15mm X 15° PEEK
0084001996191233X 27 X 13mm X 15° PEEK
0084001996190533X 27 X 11mm X 15° PEEK
0084001996189933X 27 X 19mm X 8° PEEK
0084001996188233X 27 X 17mm X 8° PEEK
0084001996187533X 27 X 15mm X 8° PEEK
0084001996186833X 27 X 13mm X 8° PEEK
0084001996185133X 27 X 11mm X 8° PEEK
0084001996184433 X 27 X 19mm X 0° PEEK
0084001996183733 X 27 X 17mm X 0° PEEK
0084001996182033 X 27 X 15mm X 0° PEEK
0084001996181333 X 27 X 13mm X 0° PEEK
0084001996180633 X 27 X 11mm X 0° PEEK
0084001996179030X 26 X 19mm X 30° PEEK
0084001996178330X 26 X 17mm X 30° PEEK
0084001996177630X 26 X 19mm X 25° PEEK
0084001996176930X 26 X 17mm X 25° PEEK
0084001996175230X 26 X 15mm X 25° PEEK
0084001996174530X 26 X 19mm X 20° PEEK
0084001996173830X 26 X 17mm X 20° PEEK
0084001996172130X 26 X 15mm X 20° PEEK
0084001996171430X 26 X 13mm X 20° PEEK
0084001996213136X 28 X 19mm X 8° PEEK
0084001996212436X 28 X 17mm X 8° PEEK
0084001996211736X 28 X 15mm X 8° PEEK
0084001996210036X 28 X 13mm X 8° PEEK
0084001996209436X 28 X 11mm X 8° PEEK

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.