510(k) K180166
K180166 is an FDA 510(k) premarket notification submitted by Life Spine, Inc. for the device "Life Spine Lumbar Fixation System (SENTRY)". The FDA issued a decision of Substantially Equivalent on Jun 22, 2018. The device falls under product code KWQ (Appliance, Fixation, Spinal Intervertebral Body), a Class II device regulated under 21 CFR 888.3060. Life Spine, Inc. has 122 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jun 22, 2018
- Date Received
- Jan 22, 2018
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Appliance, Fixation, Spinal Intervertebral Body
- Device Class
- Class II
- Regulation Number
- 888.3060
- Review Panel
- OR
- Submission Type
- 510(k)