WaveForm TA WT1-932158

GUDID 10889981243791

Interbody, 9mm x 32mm x 15mm, 8 Deg, 3D

SEASPINE ORTHOPEDICS CORPORATION

Metallic spinal interbody fusion cage
Primary Device ID10889981243791
NIH Device Record Key69bcc2f0-5133-41f0-b978-0d364fd51ef4
Commercial Distribution StatusIn Commercial Distribution
Brand NameWaveForm TA
Version Model NumberWT1-932158
Catalog NumberWT1-932158
Company DUNS079840876
Company NameSEASPINE ORTHOPEDICS CORPORATION
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 Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com

Device Identifiers

Device Issuing AgencyDevice ID
GS110889981243791 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

PHMIntervertebral fusion device with bone graft, thoracic

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-02-15
Device Publish Date2021-02-06

On-Brand Devices [WaveForm TA]

10889981243791Interbody, 9mm x 32mm x 15mm, 8 Deg, 3D
10889981243784Interbody, 9mm x 32mm x 15mm, 15 Deg, 3D
10889981243753Interbody, 9mm x 32mm x 14mm, 8 Deg, 3D
10889981243746Interbody, 9mm x 32mm x 14mm, 15 Deg, 3D
10889981243715Interbody, 9mm x 32mm x 13mm, 8 Deg, 3D
10889981243708Interbody, 9mm x 32mm x 13mm, 15 Deg, 3D
10889981243678Interbody, 9mm x 32mm x 12mm, 8 Deg, 3D
10889981243661Interbody, 9mm x 32mm x 12mm, 15 Deg, 3D
10889981243630Interbody, 9mm x 32mm x 11mm, 8 Deg, 3D
10889981243623Interbody, 9mm x 32mm x 11mm, 15 Deg, 3D
10889981243593Interbody, 9mm x 32mm x 10mm, 8 Deg, 3D
10889981243586Interbody, 9mm x 32mm x 10mm, 15 Deg, 3D
10889981243555Interbody, 9mm x 32mm x 9mm, 8 Deg, 3D
10889981243548Interbody, 9mm x 32mm x 9mm, 15 Deg, 3D
10889981243524Interbody, 9mm x 32mm x 8mm, 8 Deg, 3D
10889981243371Interbody, 9mm x 28mm x 15mm, 8 Deg, 3D
10889981243333Interbody, 9mm x 28mm x 14mm, 8 Deg, 3D
10889981243296Interbody, 9mm x 28mm x 13mm, 8 Deg, 3D
10889981243258Interbody, 9mm x 28mm x 12mm, 8 Deg, 3D
10889981243210Interbody, 9mm x 28mm x 11mm, 8 Deg, 3D
10889981243173Interbody, 9mm x 28mm x 10mm, 8 Deg, 3D
10889981243135Interbody, 9mm x 28mm x 9mm, 8 Deg, 3D
10889981243104Interbody, 9mm x 28mm x 8mm, 8 Deg, 3D
10889981242534Interbody, 11mm x 36mm x 15mm, 8 Deg, 3D
10889981242497Interbody, 11mm x 36mm x 14mm, 8 Deg, 3D
10889981242459Interbody, 11mm x 36mm x 13mm, 8 Deg, 3D
10889981242411Interbody, 11mm x 36mm x 12mm, 8 Deg, 3D
10889981242374Interbody, 11mm x 36mm x 11mm, 8 Deg, 3D
10889981242336Interbody, 11mm x 36mm x 10mm, 8 Deg, 3D
10889981242299Interbody, 11mm x 36mm x 9mm, 8 Deg, 3D
10889981242268Interbody, 11mm x 36mm x 8mm, 8 Deg, 3D

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