Primary Device ID | 10889981129729 |
NIH Device Record Key | 674f8f7f-3a61-4adb-a017-9b05610dffa1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | OsteoSurge 300 Putty |
Version Model Number | 56500010 |
Catalog Number | 56500010 |
Company DUNS | 801089152 |
Company Name | ISOTIS ORTHOBIOLOGICS, 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 | true |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | true |
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(800)550-7155 |
irvine.customerservice@seaspin | |
Phone | +1(800)550-7155 |
irvine.customerservice@seaspin |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10889981129729 [Primary] |
MBP | Filler, bone void, osteoinduction (w/o human growth factor) |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-10-21 |
10889981129729 | OsteoSurge 300 Putty, 1cc - demineralized human bone mixed with poloxamer resorbable reverse p |
M386565001001 | OsteoSurge300 Putty, 10cc - demineralized human bone mixed with poloxamer resorbable reverse ph |
M386565000501 | OsteoSurge300 Putty,5 cc - demineralized human bone mixed with poloxamer resorbable reverse pha |
M386565000251 | OsteoSurge300 Putty, 2.5cc - demineralized human bone mixed with poloxamer resorbable reverse p |