The following data is part of a premarket notification filed by Depuy, Inc. with the FDA for Nail, Intramedullary, Flexible.
| Device ID | K772081 |
| 510k Number | K772081 |
| Device Name: | NAIL, INTRAMEDULLARY, FLEXIBLE |
| Classification | Rod, Fixation, Intramedullary And Accessories |
| Applicant | DEPUY, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HSB |
| CFR Regulation Number | 888.3020 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1977-11-03 |
| Decision Date | 1977-11-11 |