FDA 510(k)
FDA class 2
Unknown
🇺🇸 United States
OPTIMESH
K Number: K014200
·
Decision Nov 26, 2003
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
11
Applicant Total
54
Review Days
705
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Basic Information
- Device Name
- OPTIMESH
- K Number
- K014200
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.3300
- Medical Specialty
- General, Plastic Surgery
- Decision
- Unknown
- Statement or Summary
- Summary
- Applicant
- Spineology, Inc.
- Date Received
- December 21, 2001
- Decision Date
- November 26, 2003
- Product Code
- EZX
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- SU
- 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 |
|---|---|---|---|
| EZX | Mesh, Surgical, Metal | FDA class 2 | General, Plastic Surgery |
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Other Clearances by Spineology, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K251302 | OptiMesh Multiplanar Expandable Interbody Fusion System | Dec 15, 2025 | Substantially Equivalent |
| K251943 | Spineology Navigation Instruments | Dec 4, 2025 | Substantially Equivalent |
| K230927 | OptiMesh Multiplanar Expandable Interbody Fusion System | Nov 1, 2023 | Substantially Equivalent |
| K231781 | OptiMesh Multiplanar Expandable Interbody Fusion System | Oct 18, 2023 | Substantially Equivalent |
| K213876 | Spineology Navigation Instruments | Aug 5, 2022 | Substantially Equivalent |
| K210155 | Duo Expandable Interbody Fusion System | Feb 19, 2021 | Substantially Equivalent |
| DEN200010 | Spineology Interbody Fusion System | Sep 18, 2020 | Unknown |
| K192047 | Rampart One Lumbar Interbody Fusion System | Aug 23, 2019 | Substantially Equivalent |
| K191091 | Rampart One Lumbar Interbody Fusion System | May 23, 2019 | Substantially Equivalent |
| K190055 | Duo Lumbar Interbody Fusion Device | Mar 7, 2019 | Substantially Equivalent |