Pro Lift Instruments 129-1012

GUDID 00190837031053

Life Spine, Inc.

Metallic spinal interbody fusion cage
Primary Device ID00190837031053
NIH Device Record Keyf7937fa7-fce4-49e1-83e4-5bea4325f7c0
Commercial Distribution StatusIn Commercial Distribution
Brand NamePro Lift Instruments
Version Model Number129-1012
Catalog Number129-1012
Company DUNS183641617
Company NameLife 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 Usefalse
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
GS100190837031053 [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

[00190837031053]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2020-02-24
Device Publish Date2019-11-07

On-Brand Devices [Pro Lift Instruments]

00190837034689151-289
00190837034672151-288
00190837031244151-214
00190837031237151-233
00190837031220151-239
00190837031213151-238
00190837031206151-237
00190837031190151-236
00190837031183151-235
00190837031176151-234
00190837031169151-162
00190837031152151-160
00190837031145151-283
00190837031138151-280
00190837031121151-277
00190837031114151-274
00190837031107151-271
00190837031091151-268
00190837031084151-265
00190837031077151-262
00190837031060129-1013
00190837031053129-1012
00190837031046129-1011
00190837031039129-1010
00190837031022129-1009
00190837031015129-1008
00190837031008129-1007
00190837030995129-1006
00190837030988112-351
00190837030971112-340
00190837030964112-222
00190837030957151-219
00190837030933114-204-4
00190837030926114-204-3
00190837030919114-204-2
00190837030902114-204-1

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