fda
19 records
FDA Device Recall: AMENDIA Omega Lumbar Interbody Fusion Device, Part Number 72-00-2-092812-11 T
2018-05-30
Class II — Omega LIF interbody implants labeled as having 11 degrees of lordosis was assembled using components manufactured with 4 degrees of lordosis.
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FDA Device Recall: Spinal Elements 5.5 x 45MM Mercury lordosed rod. A component of the Mercury Spi
2015-05-20
Class III — Some rods may not meet the appropriate traceability requirements including the lot number. Some rods were found to not include the product identification number (product number and lot nu...
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FDA Device Recall: Ti-Bond Marketing Literature/Labeling, Catalog No. LT10000, MP-14000 This devic
2015-01-14
Class II — Spinal Elements is recalling the Ti-Bond related brochures that includes LT-10000 and MP-14000 (all revisions) the content regarding the Ti-Bond coating within the literature is unsubstanti...
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FDA Recall: Spinal Elements, Inc — Class III
20130515
Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue. | Product: Mercury Spinal System DIA 5.5 x 400mm Straight Rod, Part Number: 60101-400. Intended to...
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FDA Device Recall: Mercury Spinal System DIA 5.5 x 400mm Straight Rod, Part Number: 60101-400.
2013-05-15
Class III — Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue.
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FDA Device Recall: Mercury Spinal System DIA 5.5 x 50 MM Lordosed Rod, Part Number: 60100-050.
2013-05-15
Class III — Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue.
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FDA Device Recall: Mercury Spinal System DIA 5.5 x 80mm Straight Rod, Part Number: 60101-080. I
2013-05-15
Class III — Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue.
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FDA Device Recall: Mercury Spinal System DIA 5.5 x 120mm Lordosed Rod, Part Number: 60100-120.
2013-05-15
Class III — Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue.
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FDA Device Recall: Mercury Spinal System DIA 5.5 x 90mm Straight Rod, Part Number: 60101-090. I
2013-05-15
Class III — Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue.
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FDA Device Recall: Mercury Spinal System DIA 5.5 x 50mm Straight Rod, Part Number: 60101-050. I
2013-05-15
Class III — Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue.
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FDA Device Recall: Mercury Spinal System DIA 5.5 x 110mm Straight Rod, Part Number: 60101-110.
2013-05-15
Class III — Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue.
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FDA Device Recall: Mercury Spinal System DIA 5.5 x 40mm Straight Rod, Part Number: 60101-040. I
2013-05-15
Class III — Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue.
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FDA Device Recall: Mercury Spinal System DIA 5.5 x 30mm Straight Rod, Part Number: 60101-030. I
2013-05-15
Class III — Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue.
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FDA Device Recall: Mercury Spinal System DIA 5.5 x 70 MM Lordosed Rod, Part Number: 60100-070.
2013-05-15
Class III — Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue.
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FDA Device Recall: Mercury Spinal System DIA 5.5 x 70mm Straight Rod, Part Number: 60101-070. I
2013-05-15
Class III — Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue.
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FDA Device Recall: Mercury Spinal System DIA 5.5 x 110mm Lordosed Rod, Part Number: 60100-110.
2013-05-15
Class III — Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue.
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FDA Device Recall: Mercury Spinal System DIA 5.5 x 80 MM Lordosed Rod, Part Number: 60100-080.
2013-05-15
Class III — Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue.
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FDA Device Recall: Mercury Spinal System DIA 5.5 x 100mm Straight Rod, Part Number: 60101-100.
2013-05-15
Class III — Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue.
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FDA Device Recall: Mercury Spinal System DIA 5.5 x 40 MM Lordosed Rod, Part Number: 60100-040.
2013-05-15
Class III — Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue.
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ny_corps
1 records
NY Corp: SPINAL ELEMENTS, INC.
2016-09-15
FOREIGN BUSINESS CORPORATION | County: Rockland | Jurisdiction: Delaware
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