FDA 510(k)
FDA unclassified
Substantially Equivalent
🇺🇸 United States
ACTIVATOR V SPINAL ADJUSTING INSTRUMENT
K Number: K072519
·
Decision Oct 23, 2007
Classifications
1
FEI Numbers
13
Registration Numbers
13
Same Product Code
31
Applicant Total
3
Review Days
46
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Basic Information
- Device Name
- ACTIVATOR V SPINAL ADJUSTING INSTRUMENT
- K Number
- K072519
- Device Class
- FDA unclassified
- Clearance Type
- Traditional
- Medical Specialty
- Unknown
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Activator Methods International, Ltd.
- Date Received
- September 7, 2007
- Decision Date
- October 23, 2007
- Product Code
- LXM
- Advisory Committee
- Unknown
- Review Advisory Committee
- PM
- 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 |
|---|---|---|---|
| LXM | Manipulator, Plunger-Like Joint | FDA unclassified | Unknown |
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