The following data is part of a premarket notification filed by Zimmer Inc. with the FDA for Zimmer Natural Nail System.
| Device ID | K172114 |
| 510k Number | K172114 |
| Device Name: | Zimmer Natural Nail System |
| Classification | Rod, Fixation, Intramedullary And Accessories |
| Applicant | Zimmer Inc. 345 East Main Street Warsaw, IN 46580 |
| Contact | Dhaval Saraiya |
| Correspondent | Dhaval Saraiya Zimmer Inc. 345 East Main Street Warsaw, IN 46580 |
| Product Code | HSB |
| CFR Regulation Number | 888.3020 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-07-13 |
| Decision Date | 2017-08-10 |
| Summary: | summary |