FDA.reportPublic FDA data

Arthrex®

Primary DI
00888867084254
Brand
Arthrex®
Company
ARTHREX, INC.
Model
ABS-2004-08
Catalog number
ABS-2004-08
Device description
STIMUBLAST CB PASTE, 8CC
Published
2017-02-15
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
MBPFiller, bone void, osteoinduction (w/o human growth factor)
MQVFILLER, BONE VOID, CALCIUM COMPOUND

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
MBPFiller, Bone Void, Osteoinduction (W/O Human Growth Factor)Orthopedic2
MQVFiller, Bone Void, Calcium CompoundOrthopedic2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00888867084254PrimaryGS10
M150ABS2004080SecondaryHIBCC0

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00888867084254008888670842548888670842540888867084254

GMDN Terms#

Term, Definition table
TermDefinition
Orthopaedic bone void filling material, synthetic, bioabsorbable, non-antimicrobialA bioabsorbable, implantable device made of a synthetic material(s) intended to replace bone lost through trauma, surgery, or pathological conditions (e.g., osteoporosis); it is not dedicated to dental applications and does not include an antimicrobial agent(s). It may be made of ceramics (e.g., tricalcium phosphate or hydroxyapatite), bioactive glasses/minerals/metals (e.g., strontium), or bioabsorbable polymers. Also referred to as a graft, matrix, or void filler, it typically provides an osteoconductive scaffold that promotes bone growth, and is used to fill cystic defects, repair fractures, and/or extend autogenous bone grafts. It may have adhesive properties.

Contacts#

Phone, Email table
PhoneEmail
+1(800)934-4404complaints@arthrex.com

Regulatory Flags#

DUNS number
131747628
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
true
Kit
false
Combination product
false
Lot or batch
true
Serial number
true
Manufacturing date on label
false
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00888867084384Arthrex®ABS-3005ABS-30052017-02-15
00888867084407Arthrex®ABS-3008ABS-30082017-02-15
00888867084421Arthrex®ABS-3016ABS-30162017-02-15
00888867084148Arthrex®ABS-2001-01ABS-2001-012017-02-15
00888867084155Arthrex®ABS-2001-02ABS-2001-022017-02-15
00888867084162Arthrex®ABS-2001-05ABS-2001-052017-02-15
00888867084179Arthrex®ABS-2001-10ABS-2001-102017-02-15
00888867084186Arthrex®ABS-2002-01ABS-2002-012017-02-15
00888867084193Arthrex®ABS-2002-05ABS-2002-052017-02-15
00888867084209Arthrex®ABS-2002-10ABS-2002-102017-02-15
00888867084216Arthrex®ABS-2003-05ABS-2003-052017-02-15
00888867084223Arthrex®ABS-2003-10ABS-2003-102017-02-15
00888867084230Arthrex®ABS-2004-01ABS-2004-012017-02-15
00888867084247Arthrex®ABS-2004-03ABS-2004-032017-02-15
00888867614543Arthrex®AR-S8740-16HA-SAR-S8740-16HA-S2026-10-07
00888867614550Arthrex®AR-S8740-18HA-SAR-S8740-18HA-S2026-10-07
00888867614567Arthrex®AR-S8740-20HA-SAR-S8740-20HA-S2026-10-07
00888867614574Arthrex®AR-S8740-22HA-SAR-S8740-22HA-S2026-10-07
00888867614581Arthrex®AR-S8740-24HA-SAR-S8740-24HA-S2026-10-07
00888867614598Arthrex®AR-S8740-26HA-SAR-S8740-26HA-S2026-10-07

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00199284455788BonVie+ELUTE , INC.MQV2025-08-13
00085412630731ALTAPOREApatech LtdMQV2020-11-05
00085412678146ALTAPOREApatech LtdMQV2020-11-05
00085412654362ALTAPOREApatech LtdMQV2019-12-11
00085412654379ALTAPOREApatech LtdMQV2019-12-11
00085412654386ALTAPOREApatech LtdMQV2019-12-11
00085412654393ALTAPOREApatech LtdMQV2019-12-11
00613994247612PROGENIX® PUTTY and PROGENIX® PLUSMEDTRONIC SOFAMOR DANEK, INC.MQV2019-03-29
00613994247612PROGENIX® PUTTY and PROGENIX® PLUSMEDTRONIC SOFAMOR DANEK, INC.MBP2019-03-29
00613994512758MASTERGRAFT® Mini GranulesMEDTRONIC SOFAMOR DANEK, INC.MQV2018-11-18
00613994512765MASTERGRAFT® Mini GranulesMEDTRONIC SOFAMOR DANEK, INC.MQV2018-11-18
00613994512772MASTERGRAFT® Mini GranulesMEDTRONIC SOFAMOR DANEK, INC.MQV2018-11-18
00613994512789MASTERGRAFT® Mini GranulesMEDTRONIC SOFAMOR DANEK, INC.MQV2018-11-18
00613994512796MASTERGRAFT® Mini GranulesMEDTRONIC SOFAMOR DANEK, INC.MQV2018-11-18
00613994512802MASTERGRAFT® Mini GranulesMEDTRONIC SOFAMOR DANEK, INC.MQV2018-11-18
00613994512819MASTERGRAFT® Mini GranulesMEDTRONIC SOFAMOR DANEK, INC.MQV2018-11-18
00613994512826MASTERGRAFT® Mini GranulesMEDTRONIC SOFAMOR DANEK, INC.MQV2018-11-18
00613994986467MAGNIFUSE® Bone GraftMEDTRONIC SOFAMOR DANEK, INC.MQV2015-12-01
00613994986474MAGNIFUSE® Bone GraftMEDTRONIC SOFAMOR DANEK, INC.MQV2015-12-01
00613994986481MAGNIFUSE® Bone GraftMEDTRONIC SOFAMOR DANEK, INC.MQV2015-12-01
00613994986498MAGNIFUSE® Bone GraftMEDTRONIC SOFAMOR DANEK, INC.MQV2015-12-01
00613994986504MAGNIFUSE® Bone GraftMEDTRONIC SOFAMOR DANEK, INC.MQV2015-12-01
00613994986511MAGNIFUSE® Bone GraftMEDTRONIC SOFAMOR DANEK, INC.MQV2015-12-01
00613994986528MAGNIFUSE® Bone GraftMEDTRONIC SOFAMOR DANEK, INC.MQV2015-12-01
00613994986535MAGNIFUSE® Bone GraftMEDTRONIC SOFAMOR DANEK, INC.MQV2015-12-01
00613994986542MAGNIFUSE® Bone GraftMEDTRONIC SOFAMOR DANEK, INC.MQV2015-12-01
00613994986559MAGNIFUSE® Bone GraftMEDTRONIC SOFAMOR DANEK, INC.MQV2015-12-01
00643169103986MAGNIFUSE® Bone GraftMEDTRONIC SOFAMOR DANEK, INC.MQV2015-12-01
00643169103993MAGNIFUSE® Bone GraftMEDTRONIC SOFAMOR DANEK, INC.MQV2015-12-01
00643169104006MAGNIFUSE® Bone GraftMEDTRONIC SOFAMOR DANEK, INC.MQV2015-12-01