Company
Interpore Cross International Inc
FDA 510(k) clearances and medical device recalls filed under this name. Name variants (Inc, Corp, punctuation) are merged.
0510(k) clearances (0 in 12 months)
5recalls (0 in 12 months)
2recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| No clearances in this window. | |||
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Feb 14, 2008 | Interpore Cross International Inc Allogenix; DBM in a Lipid Carrier with Calcium Granules; Model Numbers: 02-3110, Interpore Cross International, a Biomet company (Allogenix DBM products contain human tissue (allograft bone) and are Terminated |
MQV | None listed |
| Feb 14, 2008 | Interpore Cross International Inc InterGro PLUS; DBM in a Lipid Carrier with Calcium Granules; Model Numbers: DBM002, DBM005, DBM010, DBMW05 & DBMW10, Interpore Cross International, a Biomet company (lnterGro DBM products contain hu Terminated |
MQV | K031399 |
| Feb 4, 2005 | Interpore Cross International Inc Spinal Implant,
Catalog number: 1000-3000 through 1000-3015 (9 catalog numbers) Terminated |
MQP | K040168 |
| Dec 11, 2003 | Interpore Cross International Inc C-Tek Anterior Cervical Plate System: 2.3mm/4.0mm Step Drill-14mm & 2.3mm/4.0mm Step Drill-16mm Terminated |
DKA | None listed |
| Mar 20, 2003 | Interpore Cross International Inc TPS-TL Straight Drill Guide Applicator, Catalog Number 1300-9016. Terminated |
LXH | None listed |