Primary Device ID | 00846468036065 |
NIH Device Record Key | c4a4c1f5-d43f-4886-930e-36b712166991 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CONTACT® IBF PEEK VBR/IBF SYSTEM |
Version Model Number | 34-A30-16-0 |
Catalog Number | 34-A30-16-0 |
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 |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00846468036065 [Primary] |
GS1 | 00846468091484 [Primary] |
MQP | Spinal vertebral body replacement device |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-11-06 |
Device Publish Date | 2018-10-06 |
00846468036188 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
00846468036065 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
00846468036027 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
00846468035983 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |
00846468035952 | INTERBODY FUSION DEVICE / VERTEBRAL SPACER |