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 |