The following data is part of a premarket notification filed by Interpore Cross Intl. with the FDA for Geo Structure.
Device ID | K010530 |
510k Number | K010530 |
Device Name: | GEO STRUCTURE |
Classification | Spinal Vertebral Body Replacement Device |
Applicant | INTERPORE CROSS INTL. 181 TECHNOLOGY DR. Irvine, CA 92618 -2402 |
Contact | Lynn M Rodarti |
Correspondent | Lynn M Rodarti INTERPORE CROSS INTL. 181 TECHNOLOGY DR. Irvine, CA 92618 -2402 |
Product Code | MQP |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2001-02-23 |
Decision Date | 2001-08-03 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() GEO STRUCTURE 78093043 2846407 Dead/Cancelled |
EBI, LLC 2001-11-13 |