FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
TIGGES SPINAL
K Number: K811176
·
Decision May 15, 1981
Classifications
1
FEI Numbers
54
Registration Numbers
54
Same Product Code
0
Applicant Total
1
Review Days
17
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Basic Information
- Device Name
- TIGGES SPINAL
- K Number
- K811176
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 890.3490
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Applicant
- The Tiggs Co.
- Date Received
- April 28, 1981
- Decision Date
- May 15, 1981
- Product Code
- IPW
- Advisory Committee
- Physical Medicine
- 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 |
|---|---|---|---|
| IPW | Orthosis, Sacroiliac, Soft | FDA class 1 | Physical Medicine |