ASSURE Anterior Cervical Plate System, PROVIDENCE Anterior Cervical Plate System, VIP Anterior Cervical Plate System, XTEND Anterior Cervical Plate System, UNIFY Dynamic Anterior Cervical Plate System, CITADEL Anterior Lumbar Plate System, TRUSS Thoracolumbar Plate System, PLYMOUTH Thoracolumbar Plate System, SP-Fix Spinous Process Fixation Plate, RELIEVE Laminoplasty Fixation System
K181846 is the FDA 510(k) clearance record for ASSURE Anterior Cervical Plate System, PROVIDENCE Anterior Cervical Plate System, VIP Anterior Cervical Plate System, XTEND Anterior Cervical Plate System, UNIFY Dynamic Anterior Cervical Plate System, CITADEL Anterior Lumbar Plate System, TRUSS Thoracolumbar Plate System, PLYMOUTH Thoracolumbar Plate System, SP-Fix Spinous Process Fixation Plate, RELIEVE Laminoplasty Fixation System, a class II device, cleared for Globus Medical, Inc. on under FDA product code KWQ (Appliance, Fixation, Spinal Intervertebral Body). FDA records list 217 510(k) clearances for Globus Medical, Inc., from to . As of , FDA records show no recalls naming K181846.
Clearance record
- Decision date
- Received
- (118 days to decision)
- Product code
- KWQ Appliance, Fixation, Spinal Intervertebral Body
- Regulation
- 21 CFR 888.3060
- Device class
- Class II
- Review panel
- Orthopedic
- Applicant
- Globus Medical, Inc. 2560 General Armistead Ave., Audubon PA
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code KWQ
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 1 |
| January 2026 | 0 |
| February 2026 | 2 |
| March 2026 | 3 |
| April 2026 | 1 |
| May 2026 | 2 |
| June 2026 | 0 |
| July 2026 | 1 |
| August 2026 | 0 |
| September 2026 | 1 |
| October 2026 | 0 |
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