BULLET-TIP PEEK IBF SYSTEM 32-17-22-6L

GUDID 00846468090814

INTERBODY FUSION DEVICE

Pioneer Surgical Technology, Inc.

Vertebral body prosthesis
Primary Device ID00846468090814
NIH Device Record Key2f8af72c-0f43-4270-ae79-b10f6638069a
Commercial Distribution StatusIn Commercial Distribution
Brand NameBULLET-TIP PEEK IBF SYSTEM
Version Model Number32-17-22-6L
Catalog Number32-17-22-6L
Company DUNS793384496
Company NamePioneer Surgical Technology, 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 Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(386)418-8888
Emaillabeling@rtix.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com

Device Dimensions

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Device Identifiers

Device Issuing AgencyDevice ID
GS100846468090814 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

ODPIntervertebral fusion device with bone graft, cervical

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-10-16
Device Publish Date2020-10-08

On-Brand Devices [BULLET-TIP PEEK IBF SYSTEM]

00846468086664INSERTER MODULAR CLEANING
00846468077945INSTRUMENT CASE
00846468074746INSTRUMENT CASE
00846468066789SHORT, INLINE HANDLE, HUDSON
0084646806677232mm, TRIAL CADDY
0084646806676526mm, TRIAL CADDY
0084646806675822mm, TRIAL CADDY
0084646806654326MM, Lordotic Detachable Trial Caddy
0084646806653622mm, Lordotic Detachable Trial Caddy
00846468066161TRIAL SPACER
00846468066154TRIAL SPACER
00846468066147TRIAL SPACER
00846468066130TRIAL SPACER
00846468066116TRIAL SPACER
00846468066109TRIAL SPACER
00846468066093TRIAL SPACER
00846468066086TRIAL SPACER
00846468066079TRIAL SPACER
00846468066062TRIAL SPACER
00846468066055TRIAL SPACER
00846468066048TRIAL SPACER
00846468066031TRIAL SPACER
00846468066024TRIAL SPACER
00846468066017TRIAL SPACER
00846468066000TRIAL SPACER
00846468065997TRIAL SPACER
00846468065980TRIAL SPACER
00846468065973TRIAL SPACER
00846468054557INSERTER
00846468054540DETACHABLE TRIAL SPACER
00846468054533DETACHABLE TRIAL SPACER
00846468054526DETACHABLE TRIAL SPACER
00846468054519DETACHABLE TRIAL SPACER
00846468054502DETACHABLE TRIAL SPACER
00846468054496DETACHABLE TRIAL SPACER
00846468054489DETACHABLE TRIAL SPACER
00846468054472DETACHABLE TRIAL SPACER
00846468054465DETACHABLE TRIAL SPACER
00846468054458DETACHABLE TRIAL SPACER
00846468054441DETACHABLE TRIAL SPACER
00846468054434DETACHABLE TRIAL SPACER
00846468054427DETACHABLE TRIAL SPACER
00846468054410DETACHABLE TRIAL SPACER
00846468054403DETACHABLE TRIAL SPACER
00846468054397DETACHABLE TRIAL SPACER
00846468054380DETACHABLE TRIAL SPACER
00846468054373DETACHABLE TRIAL SPACER
00846468054366DETACHABLE TRIAL SPACER
00846468054359DETACHABLE TRIAL SPACER
00846468054342LOLLIPOP TRIAL SPACER

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