TLIF Curved-P, 32 x 10mm

GUDID M739PP32100

CAPTIVA SPINE, INC.

Polymeric spinal interbody fusion cage
Primary Device IDM739PP32100
NIH Device Record Key76b25532-dc53-42cb-a2bb-4726b9c61e64
Commercial Distribution StatusIn Commercial Distribution
Brand NameTLIF Curved-P, 32 x 10mm
Version Model NumberPP3210
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
HIBCCM739PP32100 [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

[M739PP32100]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-02-24
Device Publish Date2017-08-09

On-Brand Devices [TLIF Curved-P, 32 x 10mm]

M739PP3210TLIF Curved-P, 32 x 10mm

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