Primary Device ID | 00191083028842 |
NIH Device Record Key | d41f18b0-00c2-43da-9b47-9c46fc5a27ad |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Cross-Fuse® PEEK IBF System |
Version Model Number | 35-1440-13 |
Catalog Number | 35-1440-13 |
Company DUNS | 793384496 |
Company Name | Pioneer Surgical Technology, Inc. |
Device Count | 1 |
DM Exempt | true |
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(906)226-9909 |
labeling@resolvesurg.com | |
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Phone | +1(906)226-9909 |
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Phone | +1(906)226-9909 |
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Phone | +1(906)226-9909 |
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Phone | +1(906)226-9909 |
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Phone | +1(906)226-9909 |
labeling@resolvesurg.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
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Device Issuing Agency | Device ID |
---|---|
GS1 | 00191083028842 [Primary] |
GS1 | 00846468034030 [Previous] |
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 | 2022-03-10 |
Device Publish Date | 2022-03-02 |
00191083033716 | INSERTER |
00191083033709 | INSERTER, MODULAR CLEANING |
00846468040970 | INSERTER |
00191083032511 | INSERTER, MODULAR CLEANING |
00191083032504 | INSERTER, MODULAR CLEANING |
00191083032498 | TRIAL SPACER |
00846468039349 | TRIAL SPACER |
00191083032474 | TRIAL SPACER |
00846468039325 | TRIAL SPACER |
00191083032405 | TRIAL SPACER |
00191083032344 | TRIAL SPACER |
00846468038991 | TRIAL SPACER |
00191083032276 | TRIAL SPACER |
00191083033747 | TRIAL CADDY |
00191083033686 | INSTRUMENT CASE |
00191083032436 | TRIAL SPACER |
00846468039240 | TRIAL SPACER |
00191083032399 | TRIAL SPACER |
00191083032351 | TRIAL SPACER |
00191083032320 | TRIAL SPACER |
00191083032283 | TRIAL SPACER |
00846468035877 | INTERBODY FUSION DEVICE |
00846468035860 | INTERBODY FUSION DEVICE |
00191083029771 | INTERBODY FUSION DEVICE |
00191083029757 | INTERBODY FUSION DEVICE |
00846468035808 | INTERBODY FUSION DEVICE |
00191083029719 | INTERBODY FUSION DEVICE |
00191083029702 | INTERBODY FUSION DEVICE |
00846468035754 | INTERBODY FUSION DEVICE |
00846468035747 | INTERBODY FUSION DEVICE |
00191083029634 | INTERBODY FUSION DEVICE |
00191083029627 | INTERBODY FUSION DEVICE |
00191083029603 | INTERBODY FUSION DEVICE |
00191083029597 | INTERBODY FUSION DEVICE |
00846468035686 | INTERBODY FUSION DEVICE |
00191083029559 | INTERBODY FUSION DEVICE |
00846468035648 | INTERBODY FUSION DEVICE |
00191083029535 | INTERBODY FUSION DEVICE |
00191083029528 | INTERBODY FUSION DEVICE |
00191083029504 | INTERBODY FUSION DEVICE |
00191083029498 | INTERBODY FUSION DEVICE |
00191083029474 | INTERBODY FUSION DEVICE |
00191083029467 | INTERBODY FUSION DEVICE |
00191083029450 | INTERBODY FUSION DEVICE |
00846468035532 | INTERBODY FUSION DEVICE |
00191083029412 | INTERBODY FUSION DEVICE |
00846468092634 | INTERBODY FUSION DEVICE |
00191083029399 | INTERBODY FUSION DEVICE |
00846468092627 | INTERBODY FUSION DEVICE |
00846468035471 | INTERBODY FUSION DEVICE |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CROSS-FUSE 77284786 3544634 Live/Registered |
Pioneer Surgical Technology, Inc. 2007-09-20 |