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Sign in to claim this brandK2M, INC.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 600 Hope Pkwy SE, Leesburg, VA, 20175
- Website
- stryker.com
- —
- —
- [email protected]
- Phone
- +1(571)919-2000
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3008599177
- DUNS Number
- 146060863
Catalogue (24835)
Page 4 of 497| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Navigated Spine Instruments | AT01-90002 | FDA UDI | Class I | Active |
| ALEUTIAN® Interbody Systems | SP-1551-01 | FDA UDI | Class II | Active |
| CASCADIA™ Interbody System | 6101-2131606CC-G2 | FDA UDI | Class II | Active |
| CANYON Retractor Systems | AN01-91206 | FDA UDI | Class I | Unknown |
| MOJAVE Expandable Interbody System | 7012-2112410C-G2 | FDA UDI | Class II | Active |
| NILE™ Proximal Fixation System | 5401-75058 | FDA UDI | Class II | Active |
| MESA® Spinal System | 6201-P4590 | FDA UDI | Class II | Active |
| ALEUTIAN® Interbody Systems | 3303-21136MP | FDA UDI | Class II | Active |
| K2M General Instruments | PRO-1100-13 | FDA UDI | Class I | Active |
| K2M General Instruments | PRO-1044-12 | FDA UDI | Class I | Active |
| ALEUTIAN® Interbody Systems | SP-4070-06 | FDA UDI | Class II | Active |
| CANYON™ Retractor Systems | 6401-90187 | FDA UDI | Class I | Active |
| OZARK Cervical Plate System | 8801-43F64 | FDA UDI | Class II | Unknown |
| OZARK Cervical Plate System | 8801-04514D | FDA UDI | Class II | Unknown |
| CAPRI™ Corpectomy Cage System | 8101-90013 | FDA UDI | Class I | Active |
| CAPRI™ Corpectomy Cage System | 7501-21838L7-G2 | FDA UDI | Class II | Active |
| MESA® Spinal System | 6201-360105-G1 | FDA UDI | Class II | Active |
| CASCADIA™ Interbody System | 6101-2224514LL8-G2 | FDA UDI | Class II | Active |
| ALEUTIAN® Interbody Systems | 702-90389 | FDA UDI | Class II | Active |
| ALEUTIAN® Interbody Systems | 3201-90194 | FDA UDI | Class II | Active |
| EVEREST® Spinal System | SP-3076-02 | FDA UDI | Class I | Active |
| CASCADIA™ Interbody System | 6101-2185017LP-G2 | FDA UDI | Class II | Active |
| MESA® Spinal System | 801-04535 | FDA UDI | Class II | Active |
| ALEUTIAN® Interbody Systems | 602-90698 | FDA UDI | Class II | Active |
| MESA® Small Stature Spinal System | 3001-05545 | FDA UDI | Class II | Active |
| EVEREST Spinal System | 2901-66075-G1 | FDA UDI | Class II | Active |
| ALEUTIAN® Interbody Systems | 603-21224L12 | FDA UDI | Class II | Active |
| CANYON™ Retractor Systems | 6401-90142 | FDA UDI | Class I | Active |
| MESA® Small Stature Spinal System | 3001-B45500 | FDA UDI | Class II | Active |
| MESA Small Stature Spinal System | 3001-90063 | FDA UDI | Class I | Active |
| EVEREST® Spinal System | 5101-E6060 | FDA UDI | Class II | Active |
| CASPIAN® Spinal System | 1101-53580 | FDA UDI | Class II | Active |
| CAPRI™ Corpectomy Cage System | 2101-27425L15 | FDA UDI | Class II | Active |
| CASPIAN® Spinal System | 1101-04532MC | FDA UDI | Class II | Active |
| DENALI Spinal System | 101-90294 | FDA UDI | Class I | Active |
| EVEREST Spinal System | PRO-1359 | FDA UDI | Class I | Active |
| ALEUTIAN® Interbody Systems | PRO-1009-11 | FDA UDI | Class I | Active |
| YUKON OCT Spinal System | 7601-03540L-G1 | FDA UDI | Class II | Active |
| CASCADIA™ Interbody System | 6101-2141813CL30-G2 | FDA UDI | Class II | Unknown |
| CASCADIA™ Interbody System | 6101-2131613CL15-G2 | FDA UDI | Class II | Active |
| MESA Small Stature Spinal System | K2-30-2037-01 | FDA UDI | Class I | Active |
| MESA® Spinal System | 6201-35025 | FDA UDI | Class II | Active |
| ALEUTIAN® Interbody Systems | 3303-90381 | FDA UDI | Class II | Active |
| NAPA Access System | 8030-90153 | FDA UDI | Class I | Active |
| MOJAVE Expandable Interbody System | 7012-90085 | FDA UDI | Class II | Active |
| ALEUTIAN® Interbody Systems | K2-07-2057-04 | FDA UDI | Class II | Active |
| EVEREST® Spinal System | M5111-07530-G1 | FDA UDI | Class II | Active |
| MESA® Spinal System | 6201-36545 | FDA UDI | Class II | Active |
| NIAGARA Lateral Access System | PRO-1265-21 | FDA UDI | Class I | Active |
| K2M General Instruments | PRO-1079-13 | FDA UDI | Class I | Active |
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