FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
PERIOSTEAL ELEVATOR
K Number: K771747
·
Decision Sep 28, 1977
Classifications
1
FEI Numbers
226
Registration Numbers
226
Same Product Code
5
Applicant Total
303
Review Days
13
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Basic Information
- Device Name
- PERIOSTEAL ELEVATOR
- K Number
- K771747
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 872.4565
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Applicant
- Depuy, Inc.
- Date Received
- September 15, 1977
- Decision Date
- September 28, 1977
- Product Code
- EMJ
- 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 |
|---|---|---|---|
| EMJ | Elevator, Surgical, Dental | FDA class 1 | Dental |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (EMJ), ordered by most recent decision date.
ELEVATOR, ROOT, SINGLE-ENDED
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880/1 TO 890/4 VARIOUS TYPES OF PERIOTEAL ELEVATOR
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·Dental
680/1 TO 785/2 VARIOUS TYPES & SIZES OF ROOT ELEVA
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·Dental
TACTILE PLUS DENTAL ELEVATORS
FDA 510(k)
FDA Class 1
·Dental
BEACH DERIOSTEAL ELEVATOR, #2 STRAIGHT
FDA 510(k)
FDA Class 1
·Dental
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