FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Hive™ Standalone Cervical System and Hive™ C Interbody System

K Number: K254105 · Decision Feb 13, 2026
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
3
Review Days
56

Basic Information

Device Name
Hive™ Standalone Cervical System and Hive™ C Interbody System
K Number
K254105
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
NanoHive Medical, LLC
Date Received
December 19, 2025
Decision Date
February 13, 2026
Product Code
ODP
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
ODP Intervertebral Fusion Device With Bone Graft, Cervical

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (ODP), ordered by most recent decision date.

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Other Clearances by NanoHive Medical, LLC

K Number Device Name
K231241 NanoHive Medical Lumbar Interbody System
K223190 Hive™ Standalone Cervical System