The following data is part of a premarket notification filed by Howmedica Osteonics Corp. with the FDA for Dynamic Joint Distractor Ii External Fixation System.
| Device ID | K002923 |
| 510k Number | K002923 |
| Device Name: | DYNAMIC JOINT DISTRACTOR II EXTERNAL FIXATION SYSTEM |
| Classification | Appliance, Fixation, Nail/blade/plate Combination, Multiple Component, Metal Composite |
| Applicant | HOWMEDICA OSTEONICS CORP. 59 ROUTE 17 SOUTH Allendale, NJ 07401 -1677 |
| Contact | Karen Ariemma |
| Correspondent | Karen Ariemma HOWMEDICA OSTEONICS CORP. 59 ROUTE 17 SOUTH Allendale, NJ 07401 -1677 |
| Product Code | LXT |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-09-19 |
| Decision Date | 2000-12-18 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 07613327073713 | K002923 | 000 |