FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇦 Canada
PROLEX MESH
K Number: K960219
·
Decision Mar 15, 1996
Classifications
1
FEI Numbers
139
Registration Numbers
139
Same Product Code
335
Applicant Total
1
Review Days
59
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Basic Information
- Device Name
- PROLEX MESH
- K Number
- K960219
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.3300
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Advanced Surgical Innovations, Inc.
- Date Received
- January 16, 1996
- Decision Date
- March 15, 1996
- Product Code
- FTL
- Advisory Committee
- General, Plastic Surgery
- 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 |
|---|---|---|---|
| FTL | Mesh, Surgical, Polymeric | FDA class 2 | General, Plastic Surgery |
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