FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
HERNIAMESH SURGICAL MESHES
K Number: K973955
·
Decision May 11, 1998
Classifications
1
FEI Numbers
139
Registration Numbers
139
Same Product Code
335
Applicant Total
2
Review Days
207
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Basic Information
- Device Name
- HERNIAMESH SURGICAL MESHES
- K Number
- K973955
- 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
- Herniamesh
- Date Received
- October 16, 1997
- Decision Date
- May 11, 1998
- 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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Other Clearances by Herniamesh
| K Number | Device Name | ||
|---|---|---|---|
| K020652 | HERNIAMESH T-SLING | May 15, 2002 | Substantially Equivalent |