The following data is part of a premarket notification filed by Arthrex, Inc. with the FDA for Mini Tightrope.
| Device ID | K133275 |
| 510k Number | K133275 |
| Device Name: | MINI TIGHTROPE |
| Classification | Washer, Bolt Nut |
| Applicant | ARTHREX, INC. 1370 Creekside Blvd Naples, FL 34108 |
| Contact | Nancy Hoft |
| Correspondent | Nancy Hoft ARTHREX, INC. 1370 Creekside Blvd Naples, FL 34108 |
| Product Code | HTN |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-10-24 |
| Decision Date | 2014-01-30 |
| Summary: | summary |