Lordotic Cage, 25 x 7mm

GUDID M739FPL2507

Lordotic Cage, 25 x 7mm

CAPTIVA SPINE, INC.

Polymeric spinal interbody fusion cage
Primary Device IDM739FPL2507
NIH Device Record Key1566605f-7ebb-4827-a853-d77aa7c2d1a5
Commercial Distribution Discontinuation2017-07-21
Commercial Distribution StatusNot in Commercial Distribution
Brand NameLordotic Cage, 25 x 7mm
Version Model NumberFPL2507
Company DUNS836975784
Company NameCAPTIVA SPINE, 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
HIBCCM739FPL2507 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MAXIntervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[M739FPL2507]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-02-24
Device Publish Date2015-10-30

On-Brand Devices [Lordotic Cage, 25 x 7mm]

M739FPL25070Lordotic Cage, 25 x 7mm
M739FPL2507Lordotic Cage, 25 x 7mm

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