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Interventional Spine Inc

10 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
G3 Opticage Expandable Interbody Fusion Device, Model No. 9180-00, 9180-01, 9180-06, 9180- recall (Z-0941-2017)Interventional Spine Inc2017-01-03
PERPOS 2-in-1 Drills, Catalog #6070 Component Part #6070 for PERPOS 2-in-1 Drill-a canulat recall (Z-0419-2012)Interventional Spine Inc2012-01-11
Single Use PERPOS PLS System, Catalog #9045-01 Catalog#9045-01 for Single Use PERPOS PLS S recall (Z-0420-2012)Interventional Spine Inc2012-01-11
PERPOS PLS System, Single Use; CATALOG #'s 9045-01 & 9045-02. Interventional Spine, Inc. A recall (Z-0045-2012)Interventional Spine Inc2011-10-13
Reusable BONE-LOK PLS System; Catalog #'s: 9039-01 and 9039-02. Interventional Spine, Inc. recall (Z-0046-2012)Interventional Spine Inc2011-10-13
PERPOS Driver; Catalog # 6112 Interventional Spine, Inc. A cannulated, driver to be used o recall (Z-0047-2012)Interventional Spine Inc2011-10-13
PERPOS PLS, CATALOG #'s 9045-01 & 9045-02 A sterile, medical device kit consisting of the recall (Z-3033-2011)Interventional Spine Inc2011-08-18
Catalog # 9024-00 or LSW-S-3040 for 4.5mm BONE-LOK PLS Implant A sterile, canulated screw recall (Z-3034-2011)Interventional Spine Inc2011-08-18
PERPOS PLS SYSTEM, CATALOG NO. 9045-01 A sterile, medical device kit consisting of the com recall (Z-2718-2011)Interventional Spine Inc2011-07-01
PERPOS PLS SYSTEM, CATALOG NO. 9045-02 A sterile, medical device kit consisting of the com recall (Z-2719-2011)Interventional Spine Inc2011-07-01

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