FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Hive Stand-alone Anterior Lumbar Interbody System
K Number: K200541
·
Decision Apr 28, 2020
Classifications
1
FEI Numbers
253
Registration Numbers
253
Same Product Code
200
Applicant Total
3
Review Days
56
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Basic Information
- Device Name
- Hive Stand-alone Anterior Lumbar Interbody System
- K Number
- K200541
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3080
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Hd Lifesciences, LLC
- Date Received
- March 3, 2020
- Decision Date
- April 28, 2020
- Product Code
- OVD
- 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 | Device Class | Medical Specialty |
|---|---|---|---|
| OVD | Intervertebral Fusion Device With Integrated Fixation, Lumbar | FDA class 2 | Orthopedic |
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