TLIF Straight, 32 x 16mm

GUDID M739PS3216

TLIF Straight, 32 x 16mm

CAPTIVA SPINE, INC.

Polymeric spinal interbody fusion cage
Primary Device IDM739PS3216
NIH Device Record Key31f19e5c-8aad-418f-ba59-678fb50083c5
Commercial Distribution Discontinuation2017-08-11
Commercial Distribution StatusNot in Commercial Distribution
Brand NameTLIF Straight, 32 x 16mm
Version Model NumberPS3216
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
HIBCCM739PS3216 [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

[M739PS3216]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-02-24
Device Publish Date2015-08-28

On-Brand Devices [TLIF Straight, 32 x 16mm]

M739PS32160PS3216
M739PS3216TLIF Straight, 32 x 16mm

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