Primary Device ID | 00846468091507 |
NIH Device Record Key | 687d1521-2cdb-4a1a-8867-13bfc6d2eb63 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Contact PEEK IBF System |
Version Model Number | 34-A30-20-0 |
Catalog Number | 34-A30-20-0 |
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 |
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Phone | +1(386)418-8888 |
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Phone | +1(386)418-8888 |
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Phone | +1(386)418-8888 |
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Phone | +1(386)418-8888 |
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Phone | +1(906)226-9909 |
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Device Size Text, specify | 0 |
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Device Issuing Agency | Device ID |
---|---|
GS1 | 00846468091507 [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 | 2020-10-16 |
Device Publish Date | 2020-10-08 |