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The Spine Journal
Volume 2, Issue 1
, Pages
63-69
, January 2002
Anterior lumbar interbody fusion with titanium mesh cages, coralline hydroxyapatite, and demineralized bone matrix as part of a circumferential fusion
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☆ FDA device/drug status: Not approved for this indication (MOSS titanium mesh cage); approved for this indication (Pro Osteon 500R).
☆☆ Support in part or in whole was received from DePuy AcroMed.
★ Author JST acknowledges a financial relationship (grant research support from and consultant for DePuy AcroMed) which may indirectly relate to the subject of this research.
PII: S1529-9430(01)00155-3
© 2002 Elsevier Science Inc. All rights reserved.
« Previous
Next »
The Spine Journal
Volume 2, Issue 1
, Pages
63-69
, January 2002
