FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
NBD HEAD SCREW
K Number: K050377
·
Decision Apr 7, 2005
Classifications
1
FEI Numbers
250
Registration Numbers
250
Same Product Code
422
Applicant Total
4
Review Days
51
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Basic Information
- Device Name
- NBD HEAD SCREW
- K Number
- K050377
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.4560
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- New Business Development, LLC
- Date Received
- February 15, 2005
- Decision Date
- April 7, 2005
- Product Code
- HAW
- 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 |
|---|---|---|---|
| HAW | Neurological Stereotaxic Instrument | FDA class 2 | Neurology |
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