PRECICE Intramedullary Limb Lengthening System
FDA 510(k) clearance K151131 · decided 2015-06-19
Clearance details
- K-number
- K151131
- Device name
- PRECICE Intramedullary Limb Lengthening System
- Applicant
- Ellipse Technologies, Incorporated
- Decision
- Substantially Equivalent
- Date received
- 2015-04-28
- Decision date
- 2015-06-19
- Days to decision
- 52 days
- Clearance type
- Special
- Product code
- HSB
- Device class
- 2
- Regulation number
- 888.3020
- Medical specialty
- Orthopedic
- Advisory committee
- Orthopedic
- Location
- Irvine, CA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
| Record | Firm | Date |
|---|---|---|
| NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System: Model Number/I recall (Z-0319-2022) | NuVasive Specialized Orthopedics, Inc. | 2021-12-01 |
| NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System End Cap for PRE recall (Z-1349-2021) | Nuvasive Specialized Orthopedics Inc | 2021-04-05 |