FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CRANIOPLASTIC, ACRYLIC CRANIOPLASTY MATERIAL
K Number: K873689
·
Decision Oct 26, 1987
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
43
Applicant Total
279
Review Days
45
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Basic Information
- Device Name
- CRANIOPLASTIC, ACRYLIC CRANIOPLASTY MATERIAL
- K Number
- K873689
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.5300
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Applicant
- Dentsply Intl.
- Date Received
- September 11, 1987
- Decision Date
- October 26, 1987
- Product Code
- GXP
- Advisory Committee
- Neurology
- Review Advisory Committee
- NE
- 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 |
|---|---|---|---|
| GXP | Methyl Methacrylate For Cranioplasty | FDA class 2 | Neurology |
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