The following data is part of a premarket notification filed by Interpore Intl. with the FDA for Imz Intramobile Cylinder Implant System Components.
| Device ID | K863680 |
| 510k Number | K863680 |
| Device Name: | IMZ INTRAMOBILE CYLINDER IMPLANT SYSTEM COMPONENTS |
| Classification | Implant, Endosseous, Root-form |
| Applicant | INTERPORE INTL. P.O BOX 19369 Irvine, CA 92713 |
| Contact | Jo Stegwell |
| Correspondent | Jo Stegwell INTERPORE INTL. P.O BOX 19369 Irvine, CA 92713 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-09-19 |
| Decision Date | 1986-10-24 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10841307122364 | K863680 | 000 |
| 10841307118206 | K863680 | 000 |
| 10841307118152 | K863680 | 000 |
| 10841307118145 | K863680 | 000 |
| 10841307118138 | K863680 | 000 |
| 10841307118121 | K863680 | 000 |
| 10841307118114 | K863680 | 000 |
| 10841307118107 | K863680 | 000 |
| 10841307118091 | K863680 | 000 |
| 10841307118084 | K863680 | 000 |
| 10841307118077 | K863680 | 000 |
| 10841307118060 | K863680 | 000 |
| 10841307118213 | K863680 | 000 |
| 10841307118220 | K863680 | 000 |
| 10841307118756 | K863680 | 000 |
| 10841307122357 | K863680 | 000 |
| 10841307118862 | K863680 | 000 |
| 10841307118855 | K863680 | 000 |
| 10841307118848 | K863680 | 000 |
| 10841307118831 | K863680 | 000 |
| 10841307118824 | K863680 | 000 |
| 10841307118817 | K863680 | 000 |
| 10841307118800 | K863680 | 000 |
| 10841307118794 | K863680 | 000 |
| 10841307118787 | K863680 | 000 |
| 10841307118770 | K863680 | 000 |
| 10841307118053 | K863680 | 000 |