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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 26 of 497| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| MESA® Spinal System | 6201-07565 | FDA UDI | Class II | Active |
| ALEUTIAN® Interbody Systems | 3303-90120 | FDA UDI | Class II | Active |
| ALEUTIAN® Interbody Systems | 5303-21424T6 | FDA UDI | Class II | Active |
| MESA® Spinal System | SP-4182-02 | FDA UDI | Class I | Active |
| ALEUTIAN® Interbody Systems | PRO-1093-04 | FDA UDI | Class II | Active |
| ALEUTIAN Interbody Systems | PRO-1242 | FDA UDI | Class I | Active |
| ALEUTIAN Interbody Systems | K2-32-2051-12 | FDA UDI | Class I | Active |
| EVEREST® Spinal System | M5111-34570T | FDA UDI | Class II | Active |
| Q Pedicle Instruments | 48132000 | FDA UDI | Class II | Active |
| EVEREST® Spinal System | SP-4227-03 | FDA UDI | Class I | Active |
| Navigated Spine Instruments | 7601-N90009-K | FDA UDI | Class I | Active |
| OZARK Cervical Plate System | SP-4174-02 | FDA UDI | Class I | Active |
| K2M Fenestrated Tap System | SP-4029-01 | FDA UDI | Class II | Active |
| K2M General Instruments | AG01-96083 | FDA UDI | Class I | Active |
| CANYON Retractor Systems | AN01-92207 | FDA UDI | Class I | Unknown |
| DENALI® MI Spinal System | 1001-A55200-G1 | FDA UDI | Class II | Active |
| OZARK Cervical Plate System | 8801-14310D | FDA UDI | Class II | Unknown |
| MESA® Spinal System | 6201-P4550 | FDA UDI | Class II | Active |
| MESA® Spinal System | 6201-37595-G1 | FDA UDI | Class II | Active |
| MESA® Spinal System | 6201-065110-G1 | FDA UDI | Class II | Active |
| ALEUTIAN® Interbody Systems | 3303-21528W | FDA UDI | Class II | Active |
| MESA® Spinal System | 6201-04545-G1 | FDA UDI | Class II | Active |
| CHESAPEAKE® Stabilization System | 2013-21130L20 | FDA UDI | Class II | Active |
| ALEUTIAN® Interbody Systems | 403-22010 | FDA UDI | Class II | Active |
| NIAGARA Lateral Access System | PRO-1265-41 | FDA UDI | Class I | Active |
| CANYON™ Retractor Systems | AN01-92321 | FDA UDI | Class I | Active |
| OZARK Cervical Plate System | AA01-43F36V | FDA UDI | Class II | Active |
| CAPRI Corpectomy Cage System | 2101-26222L0 | FDA UDI | Class II | Active |
| PYRENEES® Cervical Plate System | 5901-14714C | FDA UDI | Class II | Unknown |
| CAPRI™ Corpectomy Cage System | 2112-90008 | FDA UDI | Class II | Active |
| CHESAPEAKE Stabilization System | 2008-90046 | FDA UDI | Class I | Active |
| CASPIAN® Spinal System | 1101-04512MC | FDA UDI | Class II | Unknown |
| ALEUTIAN® Interbody Systems | 602-90364 | FDA UDI | Class II | Active |
| OZARK Cervical Plate System | AA01-43F41V | FDA UDI | Class II | Active |
| NIAGARA® Lateral Access System | PRO-1099-02 | FDA UDI | Class I | Active |
| EVEREST® Spinal System | PRO-1004-02 | FDA UDI | Class I | Active |
| MESA® Small Stature Spinal System | 3011-645150-G1 | FDA UDI | Class II | Active |
| MESA® Spinal System | 6201-P6595 | FDA UDI | Class II | Active |
| CAPRI™ Corpectomy Cage System | 7501-21644L30-G2 | FDA UDI | Class II | Active |
| ALEUTIAN Interbody Systems | 3303-90035 | FDA UDI | Class I | Active |
| CAPRI™ Corpectomy Cage System | 7501-21622L20-G2 | FDA UDI | Class II | Active |
| MESA® Spinal System | 6201-31260-G1 | FDA UDI | Class II | Active |
| NIAGARA® Lateral Access System | PRO-1010 | FDA UDI | Class I | Active |
| ALEUTIAN Cervical | SP-4256-01 | FDA UDI | Class I | Active |
| YUKON OCT Spinal System | 7601-90018 | FDA UDI | Class I | Active |
| ALEUTIAN® Interbody Systems | 3201-90321 | FDA UDI | Class I | Active |
| EVEREST Spinal System | 2901-90032 | FDA UDI | Class I | Active |
| CASCADIA™ Interbody System | 6101-2225508LP-G2 | FDA UDI | Class II | Active |
| CASPIAN® Spinal System | 1101-03532MC | FDA UDI | Class II | Unknown |
| ALEUTIAN® Interbody Systems | 602-90722 | FDA UDI | Class II | Active |
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