The following data is part of a premarket notification filed by Smith & Nephew Richards, Inc. with the FDA for The Modular Nail.
| Device ID | K933027 |
| 510k Number | K933027 |
| Device Name: | THE MODULAR NAIL |
| Classification | Rod, Fixation, Intramedullary And Accessories |
| Applicant | SMITH & NEPHEW RICHARDS, INC. 1450 BROOKS RD. Memphis, TN 38116 |
| Contact | Thomas L Craig |
| Correspondent | Thomas L Craig SMITH & NEPHEW RICHARDS, INC. 1450 BROOKS RD. Memphis, TN 38116 |
| Product Code | HSB |
| CFR Regulation Number | 888.3020 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-06-22 |
| Decision Date | 1994-02-22 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 23596010061915 | K933027 | 000 |
| 03596010061768 | K933027 | 000 |
| 03596010061775 | K933027 | 000 |
| 03596010061782 | K933027 | 000 |
| 03596010061799 | K933027 | 000 |
| 03596010061805 | K933027 | 000 |
| 03596010061812 | K933027 | 000 |
| 03596010061829 | K933027 | 000 |
| 03596010061836 | K933027 | 000 |
| 03596010061843 | K933027 | 000 |
| 03596010061850 | K933027 | 000 |
| 03596010061867 | K933027 | 000 |
| 03596010061874 | K933027 | 000 |
| 03596010061881 | K933027 | 000 |
| 03596010061898 | K933027 | 000 |
| 03596010061904 | K933027 | 000 |
| 03596010061751 | K933027 | 000 |