The following data is part of a premarket notification filed by Nuvasive Specialized Orthopedics, Inc. with the FDA for Precice Intramedullary Limb Lengthening System.
| Device ID | K170169 |
| 510k Number | K170169 |
| Device Name: | PRECICE Intramedullary Limb Lengthening System |
| Classification | Rod, Fixation, Intramedullary And Accessories |
| Applicant | NuVasive Specialized Orthopedics, Inc. 101 Enterprise, Suite 100 Aliso Viejo, CA 92656 |
| Contact | Cora Sim |
| Correspondent | Cora Sim NuVasive Specialized Orthopedics, Inc. 101 Enterprise, Suite 100 Aliso Viejo, CA 92656 |
| Product Code | HSB |
| CFR Regulation Number | 888.3020 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-01-19 |
| Decision Date | 2017-06-09 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00887517001344 | K170169 | 000 |
| 00887517990105 | K170169 | 000 |
| 00887517945327 | K170169 | 000 |
| 00887517945310 | K170169 | 000 |
| 00887517945303 | K170169 | 000 |