LAT-FUSE™* LATERAL PLATE SYSTEM 38-60-70

GUDID 00846468013103

SELF-TAPPING SCREW

Pioneer Surgical Technology, Inc.

Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable
Primary Device ID00846468013103
NIH Device Record Key03d1f84b-820b-49fe-b1b4-74a0579b4a68
Commercial Distribution StatusIn Commercial Distribution
Brand NameLAT-FUSE™* LATERAL PLATE SYSTEM
Version Model Number38-60-70
Catalog Number38-60-70
Company DUNS793384496
Company NamePioneer Surgical 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 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
GS100846468013103 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KWQAPPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00846468013103]

Moist Heat or Steam Sterilization


[00846468013103]

Moist Heat or Steam Sterilization


[00846468013103]

Moist Heat or Steam Sterilization


[00846468013103]

Moist Heat or Steam Sterilization


[00846468013103]

Moist Heat or Steam Sterilization


[00846468013103]

Moist Heat or Steam Sterilization


[00846468013103]

Moist Heat or Steam Sterilization


[00846468013103]

Moist Heat or Steam Sterilization


[00846468013103]

Moist Heat or Steam Sterilization


[00846468013103]

Moist Heat or Steam Sterilization


[00846468013103]

Moist Heat or Steam Sterilization


[00846468013103]

Moist Heat or Steam Sterilization


[00846468013103]

Moist Heat or Steam Sterilization


[00846468013103]

Moist Heat or Steam Sterilization


[00846468013103]

Moist Heat or Steam Sterilization


[00846468013103]

Moist Heat or Steam Sterilization


[00846468013103]

Moist Heat or Steam Sterilization


[00846468013103]

Moist Heat or Steam Sterilization


[00846468013103]

Moist Heat or Steam Sterilization


[00846468013103]

Moist Heat or Steam Sterilization


[00846468013103]

Moist Heat or Steam Sterilization


[00846468013103]

Moist Heat or Steam Sterilization


[00846468013103]

Moist Heat or Steam Sterilization


[00846468013103]

Moist Heat or Steam Sterilization


[00846468013103]

Moist Heat or Steam Sterilization


[00846468013103]

Moist Heat or Steam Sterilization


[00846468013103]

Moist Heat or Steam Sterilization


[00846468013103]

Moist Heat or Steam Sterilization


[00846468013103]

Moist Heat or Steam Sterilization


[00846468013103]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-01-13

On-Brand Devices [LAT-FUSE™* LATERAL PLATE SYSTEM]

00846468049249LATERAL PLATE
00846468049232LATERAL PLATE
00846468014414LATERAL PLATE
00846468014407LATERAL PLATE
00846468014391LATERAL PLATE
00846468014384LATERAL PLATE
00846468014377LATERAL PLATE
00846468014360LATERAL PLATE
00846468014353LATERAL PLATE
00846468014346LATERAL PLATE
00846468014339LATERAL PLATE
00846468014322LATERAL PLATE
00846468014315LATERAL PLATE
00846468014308SELF-DRILLING SCREW
00846468014292SELF-DRILLING SCREW
00846468014285SELF-DRILLING SCREW
00846468014278SELF-DRILLING SCREW
00846468014261SELF-DRILLING SCREW
00846468014254SELF-DRILLING SCREW
00846468014247SELF-DRILLING SCREW
00846468014230SELF-DRILLING SCREW
00846468014223SELF-DRILLING SCREW
00846468014216SELF-DRILLING SCREW
00846468014209SELF-DRILLING SCREW
00846468014193SELF-DRILLING SCREW
00846468014186SELF-DRILLING SCREW
00846468014179SELF-DRILLING SCREW
00846468014162SELF-DRILLING SCREW
00846468014155SELF-DRILLING SCREW
00846468014148SELF-DRILLING SCREW
00846468014131SELF-DRILLING SCREW
00846468014124SELF-DRILLING SCREW
00846468014117SELF-DRILLING SCREW
00846468014100SELF-DRILLING SCREW
00846468014094SELF-DRILLING SCREW
00846468014087SELF-DRILLING SCREW
00846468014070SELF-DRILLING SCREW
00846468014063SELF-DRILLING SCREW
00846468014056SELF-DRILLING SCREW
00846468014049SELF-DRILLING SCREW
00846468014032SELF-DRILLING SCREW
00846468014025SELF-DRILLING SCREW
00846468014018SELF-DRILLING SCREW
00846468014001SELF-DRILLING SCREW
00846468013998SELF-DRILLING SCREW
00846468013981SELF-DRILLING SCREW
00846468013974SELF-DRILLING SCREW
00846468013967SELF-DRILLING SCREW
00846468013950SELF-DRILLING SCREW
00846468013943SELF-DRILLING SCREW

Trademark Results [LAT-FUSE]

Mark Image

Registration | Serial
Company
Trademark
Application Date
LAT-FUSE
LAT-FUSE
85605450 5022703 Live/Registered
Pioneer Surgical Technology, Inc.
2012-04-23

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