CONVENTUS DRS
Plate, Fixation, Bone
CONVENTUS ORTHOPAEDICS
The following data is part of a premarket notification filed by Conventus Orthopaedics with the FDA for Conventus Drs.
Pre-market Notification Details
| Device ID | K131552 |
| 510k Number | K131552 |
| Device Name: | CONVENTUS DRS |
| Classification | Plate, Fixation, Bone |
| Applicant | CONVENTUS ORTHOPAEDICS 10200 73RD AVENUE NORTH STE 122 Maple Grove, MN 55369 |
| Contact | Kent Lind |
| Correspondent | Kent Lind CONVENTUS ORTHOPAEDICS 10200 73RD AVENUE NORTH STE 122 Maple Grove, MN 55369 |
| Product Code | HRS |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-05-30 |
| Decision Date | 2014-02-12 |
| Summary: | summary |
Trademark Results [CONVENTUS DRS]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 CONVENTUS DRS 86119717 4575033 Live/Registered |
Conventus Orthopaedics, Inc. 2013-11-15 |
 CONVENTUS DRS 85645436 4485849 Live/Registered |
Conventus Orthopaedics, Inc. 2012-06-07 |
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