Interpore Cross International Inc
5 FDA 510(k) clearances · Recalling firm
◉ Watch Interpore Cross International Inc
| Record | Firm | Date |
|---|---|---|
| InterGro PLUS; DBM in a Lipid Carrier with Calcium Granules; Model Numbers: DBM002, DBM005 recall (Z-0618-2008) | Interpore Cross International Inc | 2008-02-14 |
| Allogenix; DBM in a Lipid Carrier with Calcium Granules; Model Numbers: 02-3110, Interpore recall (Z-0619-2008) | Interpore Cross International Inc | 2008-02-14 |
| Spinal Implant, Catalog number: 1000-3000 through 1000-3015 (9 catalog numbers) recall (Z-0530-05) | Interpore Cross International Inc | 2005-02-04 |
| C-Tek Anterior Cervical Plate System: 2.3mm/4.0mm Step Drill-14mm & 2.3mm/4.0mm Step Drill recall (Z-0211-04) | Interpore Cross International Inc | 2003-12-11 |
| TPS-TL Straight Drill Guide Applicator, Catalog Number 1300-9016. recall (Z-0659-03) | Interpore Cross International Inc | 2003-03-20 |
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Every clearance here is in the API, with alerts when new ones post.