The following data is part of a premarket notification filed by Arthrex, Inc. with the FDA for Anthrex Titanium Opening Wedge Osteotomy System.
| Device ID | K032187 |
| 510k Number | K032187 |
| Device Name: | ANTHREX TITANIUM OPENING WEDGE OSTEOTOMY SYSTEM |
| Classification | Plate, Fixation, Bone |
| Applicant | ARTHREX, INC. 2885 SOUTH HORSESHOE DR. Naples, FL 34104 |
| Contact | Sally Foust |
| Correspondent | Sally Foust ARTHREX, INC. 2885 SOUTH HORSESHOE DR. Naples, FL 34104 |
| Product Code | HRS |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-07-17 |
| Decision Date | 2003-09-22 |
| Summary: | summary |