510(k) K172032
K172032 is an FDA 510(k) premarket notification submitted by Aesculap Implants Systems, Inc. for the device "Modulift Vertebral Body Replacement (VBR) System". The FDA issued a decision of Substantially Equivalent on November 20, 2017. The device falls under product code PLR (Spinal Vertebral Body Replacement Device - Cervical), a Class II device regulated under 21 CFR 888.3060. Aesculap Implants Systems, Inc. has at least 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 20, 2017
- Date Received
- July 5, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Spinal Vertebral Body Replacement Device - Cervical
- Device Class
- Class II
- Regulation Number
- 888.3060
- Review Panel
- OR
- Submission Type
Vertebral body replacement in the cervical spine.