FDA 510(k)
FDA class 2
Substantially Equivalent
🇩🇰 Denmark
3Shape Abutment Designer Software
K Number: K151455
·
Decision Sep 6, 2016
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
7
Applicant Total
8
Review Days
463
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Basic Information
- Device Name
- 3Shape Abutment Designer Software
- K Number
- K151455
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3630
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- 3Shape A/S
- Date Received
- June 1, 2015
- Decision Date
- September 6, 2016
- Product Code
- PNP
- 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 |
|---|---|---|---|
| PNP | Dental Abutment Design Software For Dental Laboratory | FDA class 2 | Dental |
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Other Clearances by 3Shape A/S
| K Number | Device Name | ||
|---|---|---|---|
| K200100 | Abutment Design | Oct 7, 2020 | Substantially Equivalent |
| K191911 | 3Shape Splint Design | Nov 27, 2019 | Substantially Equivalent |
| K180941 | Ortho System | Oct 17, 2018 | Substantially Equivalent |
| K171634 | Ortho System | Jan 17, 2018 | Substantially Equivalent |
| K163677 | Ortho System | Apr 20, 2017 | Substantially Equivalent |
| K161884 | Ortho System | Apr 19, 2017 | Substantially Equivalent |
| K152086 | 3Shape Ortho System | Apr 28, 2016 | Substantially Equivalent |