The following data is part of a premarket notification filed by Integra Lifesciences Corporation with the FDA for Panta 2 Arthrodesis Nail System.
| Device ID | K181639 |
| 510k Number | K181639 |
| Device Name: | Panta 2 Arthrodesis Nail System |
| Classification | Rod, Fixation, Intramedullary And Accessories |
| Applicant | Integra Lifesciences Corporation 11101 Metric Blvd. Austin, TX 78758 |
| Contact | Blesson Abraham |
| Correspondent | Blesson Abraham Integra Lifesciences Corporation 11101 Metric Blvd. Austin, TX 78758 |
| Product Code | HSB |
| CFR Regulation Number | 888.3020 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-06-21 |
| Decision Date | 2018-11-02 |
| Summary: | summary |