FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
BIOMESH P1 AND BIOMESH PLUG AND PATCH
K Number: K002479
·
Decision Oct 19, 2000
Classifications
1
FEI Numbers
139
Registration Numbers
139
Same Product Code
335
Applicant Total
1
Review Days
69
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Basic Information
- Device Name
- BIOMESH P1 AND BIOMESH PLUG AND PATCH
- K Number
- K002479
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.3300
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Cousin Biotech S.A.R.L
- Date Received
- August 11, 2000
- Decision Date
- October 19, 2000
- 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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