FDA 510(k)
FDA unclassified
Substantially Equivalent
🇺🇸 United States
SILICONE TISSUE EXPANDER
K Number: K070303
·
Decision Jun 22, 2007
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
54
Applicant Total
1
Review Days
142
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Basic Information
- Device Name
- SILICONE TISSUE EXPANDER
- K Number
- K070303
- Device Class
- FDA unclassified
- Clearance Type
- Traditional
- Medical Specialty
- Unknown
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Specialty Surgical Products
- Date Received
- January 31, 2007
- Decision Date
- June 22, 2007
- Product Code
- LCJ
- Advisory Committee
- Unknown
- Review Advisory Committee
- SU
- 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 |
|---|---|---|---|
| LCJ | Tissue Expander And Accessories | FDA unclassified | Unknown |
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