The following data is part of a premarket notification filed by Synthes (usa) with the FDA for Synthes (usa) Low-profile Wrist Fixator.
| Device ID | K051049 |
| 510k Number | K051049 |
| Device Name: | SYNTHES (USA) LOW-PROFILE WRIST FIXATOR |
| Classification | Appliance, Fixation, Nail/blade/plate Combination, Multiple Component |
| Applicant | SYNTHES (USA) 1302 WRIGHTS LANE EAST West Chester, PA 19380 |
| Contact | Kathy Anderson |
| Correspondent | Kathy Anderson SYNTHES (USA) 1302 WRIGHTS LANE EAST West Chester, PA 19380 |
| Product Code | KTT |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2005-04-25 |
| Decision Date | 2005-07-13 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| H67903304322S0 | K051049 | 000 |
| H67903304320S0 | K051049 | 000 |
| H67903304222S0 | K051049 | 000 |
| H67903304220S0 | K051049 | 000 |