FormaGraft

GUDID 00887517238450

FormaGraft® XL Blocks, Small

Nuvasive, Inc.

Bone matrix implant, composite
Primary Device ID00887517238450
NIH Device Record Key72f04ec5-1aae-4803-b211-81ed7238778c
Commercial Distribution StatusIn Commercial Distribution
Brand NameFormaGraft
Version Model Number5010085
Company DUNS053950783
Company NameNuvasive, 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 Datetrue
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(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100887517238450 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MQVFILLER, BONE VOID, CALCIUM COMPOUND

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-11-19

On-Brand Devices [FormaGraft]

00887517517500Booth Biologics Tradeshow
00887517239372FormaGraft® Strips, Small
00887517239365FormaGraft® Strips, Large
00887517239310FormaGraft® XL Blocks, Large
00887517238450FormaGraft® XL Blocks, Small
00887517238443FormaGraft® Granules, 20cc
00887517238436FormaGraft® Granules, 10cc
00887517238412FormaGraft® Granules, 5cc
00887517238429FormaGraft BMA Needle, 8" Packaged
00887517237392FormaGraft BMA Needle, 6-Port (1)

Trademark Results [FormaGraft]

Mark Image

Registration | Serial
Company
Trademark
Application Date
FORMAGRAFT
FORMAGRAFT
78825902 3193633 Dead/Cancelled
NUVASIVE, INC.
2006-02-28

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