MCAFFEE UNIVERSAL SPINAL SYSTEM (MUSS)
FDA 510(k) clearance K901507 · decided 1992-01-28
Clearance details
- K-number
- K901507
- Device name
- MCAFFEE UNIVERSAL SPINAL SYSTEM (MUSS)
- Applicant
- Kirschner Medical Corp.
- Decision
- Substantially Equivalent
- Date received
- 1990-03-30
- Decision date
- 1992-01-28
- Days to decision
- 669 days
- Clearance type
- Traditional
- Product code
- KWQ
- Device class
- 2
- Regulation number
- 888.3060
- Medical specialty
- Orthopedic
- Advisory committee
- Orthopedic
- Location
- Timonium, MD, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Kirschner Medical Corp.
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| Palisades™ Buttress Plate System (K261309) | Bethesda Medical Devices, LLC | 2026-07-16 |
| ARIES Anterior Cervical Plate Systems (K252776) | ZheJiang Decans Medical Devices Co., Ltd. | 2026-05-14 |
| CastleLoc-P Anterior Cervical Plate System (K261112) | L&K BIOMED Co., Ltd. | 2026-05-06 |
| corra™ cervical plating system (K260570) | Carlsmed, Inc. | 2026-04-22 |
| VyPlate™ Anterior Cervical Plate System (K260697) | Vy Spine, LLC | 2026-03-27 |
| ANTERIS Thoracolumbar Plate System (K260015) | SpineCraft | 2026-03-04 |
| PathLoc Lumbar Plate System (K251940) | L&K BIOMED Co., Ltd. | 2026-03-03 |
| Aster (K254182) | Osteonic Co., Ltd. | 2026-02-26 |
| Lumbar Spine Truss System - Plating Solution (LSTS-PS) (K253201) | 4Web, Inc. | 2026-02-12 |
| aprevo® cervical plating system (K252611) | Carlsmed, Inc. | 2025-12-22 |
| Proximity Anterior Cervical Plate System; Segmental Plating System (SPS) (K251965) | Alphatec Spine, Inc. | 2025-08-28 |
| Resolve Anterior Cervical Plate System (K251436) | Pioneer Surgical Technology, Inc. | 2025-07-11 |
Recalls involving this device
No recalls on record reference this clearance.