FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇦 Canada
ADI/B/*/HA-2 STAGE OSSEO. HYDRO. DENTAL IMPLANT
K Number: K873939
·
Decision Mar 15, 1988
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
2
Review Days
169
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Basic Information
- Device Name
- ADI/B/*/HA-2 STAGE OSSEO. HYDRO. DENTAL IMPLANT
- K Number
- K873939
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3640
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Applicant
- Anchor Implants , Ltd.
- Date Received
- September 28, 1987
- Decision Date
- March 15, 1988
- Product Code
- DZE
- 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 |
|---|---|---|---|
| DZE | Implant, Endosseous, Root-Form | FDA class 2 | Dental |
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Other Clearances by Anchor Implants , Ltd.
| K Number | Device Name | ||
|---|---|---|---|
| K871887 | ANCHOR IIA/2 STAGE OSSEO. TIT. 6/4 ALLOY IMPLANT | Jul 31, 1987 | Substantially Equivalent |