CONTACT™* IBF PEEK VBR/IBF SYSTEM 34-A40-14-8
GUDID 00846468036416
INTERBODY FUSION DEVICE / VERTEBRAL SPACER
Pioneer Surgical Technology, Inc.
Polymeric spinal fusion cage, sterile| Primary Device ID | 00846468036416 |
| NIH Device Record Key | 8eef1c53-86ad-4669-976e-69eb82066973 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CONTACT™* IBF PEEK VBR/IBF SYSTEM |
| Version Model Number | 34-A40-14-8 |
| Catalog Number | 34-A40-14-8 |
| Company DUNS | 793384496 |
| Company Name | Pioneer Surgical Technology, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | +1(386)418-8888 |
| labeling@rtix.com | |
| Phone | +1(386)418-8888 |
| labeling@rtix.com | |
| Phone | +1(386)418-8888 |
| labeling@rtix.com | |
| Phone | +1(386)418-8888 |
| labeling@rtix.com | |
| Phone | +1(386)418-8888 |
| labeling@rtix.com | |
| Phone | +1(386)418-8888 |
| labeling@rtix.com | |
| Phone | +1(386)418-8888 |
| labeling@rtix.com | |
| Phone | +1(386)418-8888 |
| labeling@rtix.com | |
| Phone | +1(386)418-8888 |
| labeling@rtix.com | |
| Phone | +1(386)418-8888 |
| labeling@rtix.com | |
| Phone | +1(386)418-8888 |
| labeling@rtix.com | |
| Phone | +1(386)418-8888 |
| labeling@rtix.com | |
| Phone | +1(386)418-8888 |
| labeling@rtix.com | |
| Phone | +1(386)418-8888 |
| labeling@rtix.com | |
| Phone | +1(386)418-8888 |
| labeling@rtix.com | |
| Phone | +1(386)418-8888 |
| labeling@rtix.com | |
| Phone | +1(386)418-8888 |
| labeling@rtix.com | |
| Phone | +1(386)418-8888 |
| labeling@rtix.com | |
| Phone | +1(906)226-9909 |
| labeling@resolvesurg.com | |
| Phone | +1(386)418-8888 |
| labeling@rtix.com | |
| Phone | +1(906)226-9909 |
| labeling@resolvesurg.com | |
| Phone | +1(386)418-8888 |
| labeling@rtix.com | |
| Phone | +1(906)226-9909 |
| labeling@resolvesurg.com | |
| Phone | +1(386)418-8888 |
| labeling@rtix.com | |
| Phone | +1(906)226-9909 |
| labeling@resolvesurg.com | |
| Phone | +1(386)418-8888 |
| labeling@rtix.com | |
| Phone | +1(906)226-9909 |
| labeling@resolvesurg.com | |
| Phone | +1(386)418-8888 |
| labeling@rtix.com | |
| Phone | +1(906)226-9909 |
| labeling@resolvesurg.com | |
| Phone | +1(386)418-8888 |
| labeling@rtix.com | |
| Phone | +1(906)226-9909 |
| labeling@resolvesurg.com | |
| Phone | +1(386)418-8888 |
| labeling@rtix.com | |
| Phone | +1(906)226-9909 |
| labeling@resolvesurg.com | |
| Phone | +1(386)418-8888 |
| labeling@rtix.com | |
| Phone | +1(906)226-9909 |
| labeling@resolvesurg.com | |
| Phone | +1(386)418-8888 |
| labeling@rtix.com | |
| Phone | +1(906)226-9909 |
| labeling@resolvesurg.com | |
| Phone | +1(386)418-8888 |
| labeling@rtix.com | |
| Phone | +1(906)226-9909 |
| labeling@resolvesurg.com | |
| Phone | +1(386)418-8888 |
| labeling@rtix.com | |
| Phone | +1(906)226-9909 |
| labeling@resolvesurg.com | |
| Phone | +1(386)418-8888 |
| labeling@rtix.com | |
| Phone | +1(906)226-9909 |
| labeling@resolvesurg.com | |
| Phone | +1(386)418-8888 |
| labeling@rtix.com | |
| Phone | +1(906)226-9909 |
| labeling@resolvesurg.com | |
| Phone | +1(386)418-8888 |
| labeling@rtix.com | |
| Phone | +1(906)226-9909 |
| labeling@resolvesurg.com | |
| Phone | +1(386)418-8888 |
| labeling@rtix.com | |
| Phone | +1(906)226-9909 |
| labeling@resolvesurg.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00846468036416 [Primary] |
| GS1 | 00846468091347 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K133455
FDA Product Code
| MAX | Intervertebral fusion device with bone graft, lumbar |
| ODP | Intervertebral fusion device with bone graft, cervical |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-06-25 |
On-Brand Devices [CONTACT™* IBF PEEK VBR/IBF SYSTEM]
| 00846468036508 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036492 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036485 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036478 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036461 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036454 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036447 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036430 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036423 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036416 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036409 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036393 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036386 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036379 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036362 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036355 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036348 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036331 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036324 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036317 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036300 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036294 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036287 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036270 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036263 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036256 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036249 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036232 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036225 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036218 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036201 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036195 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036171 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036164 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036157 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036133 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036126 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036119 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036096 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036089 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036072 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036058 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036041 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036034 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036010 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468036003 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468035990 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468035976 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
| 00846468035969 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
Trademark Results [CONTACT]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 CONTACT 98757340 not registered Live/Pending |
Kids Stop LLC 2024-09-18 |
 CONTACT 98663814 not registered Live/Pending |
Contact Broadheads LLC 2024-07-24 |
 CONTACT 97749208 not registered Live/Pending |
Contact Wearables LLC 2023-01-10 |
 CONTACT 97391779 not registered Live/Pending |
Immerse Yourself Entertainment 2022-05-02 |
 CONTACT 88481644 5897359 Live/Registered |
CNS OUTDOOR TECHNOLOGIES, LLC 2019-06-20 |
 CONTACT 88319862 not registered Live/Pending |
Antowne K. Clower 2019-02-28 |
 CONTACT 88300050 5901163 Live/Registered |
Play'n GO Marks Ltd. 2019-02-13 |
 CONTACT 87841036 not registered Dead/Abandoned |
Orsmond, Albert N. 2018-03-20 |
 CONTACT 86902846 not registered Dead/Abandoned |
Pling, Ali Ibrahim 2016-02-09 |
 CONTACT 86902844 5045013 Live/Registered |
Pling, Ali Ibrahim 2016-02-09 |
 CONTACT 86754741 not registered Dead/Abandoned |
NLU Products, L.L.C. 2015-09-11 |
 CONTACT 86744575 5223848 Live/Registered |
NLU Products, L.L.C. 2015-09-01 |
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