FDA 510(k)
FDA class 2
Substantially Equivalent
🇰🇷 South Korea
GBR System
K Number: K143730
·
Decision Jun 10, 2015
Classifications
1
FEI Numbers
110
Registration Numbers
110
Same Product Code
288
Applicant Total
18
Review Days
163
Basic Information
- Device Name
- GBR System
- K Number
- K143730
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.4760
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- JEIL MEDICAL CORPORATION
- Date Received
- December 29, 2014
- Decision Date
- June 10, 2015
- Product Code
- JEY
- Advisory Committee
- Dental
- Review Advisory Committee
- DE
- 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 |
|---|---|---|---|
| JEY | Plate, Bone | FDA class 2 | Dental |
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Other Clearances by JEIL MEDICAL CORPORATION
| K Number | Device Name | ||
|---|---|---|---|
| K161335 | Dual Top Screw System | Feb 23, 2017 | Substantially Equivalent |
| K163308 | SMARTO | Dec 27, 2016 | Substantially Equivalent |
| K161864 | ARIX Foot System | Aug 2, 2016 | Substantially Equivalent |
| K141452 | LEFORTE NEURO SYSTEM BONE PLATE AND SCREW | Jul 2, 2014 | Substantially Equivalent |
| K132876 | ARIX HAND LOCKING SYSTEM | Dec 18, 2013 | Substantially Equivalent |
| K131566 | ARIX HAND SYSTEM | Nov 4, 2013 | Substantially Equivalent |
| K131311 | ARIX FOOT SYSTEM | Sep 5, 2013 | Substantially Equivalent |
| K112812 | LEFORTE NEURO SYSTEM BONE PLATE | Feb 22, 2012 | Substantially Equivalent |
| K101902 | J TAC MODEL JT-MD-035, JT-MD-040, JT-MD-045, JT-CL-030 | Feb 8, 2011 | Substantially Equivalent |
| K103778 | LEFORTE NEURO SYSTEM BONE PLATE | Jan 26, 2011 | Substantially Equivalent |