FDA 510(k)
FDA class 2
Substantially Equivalent
🇮🇹 Italy
Assut Filbloc Permanent Sutures
K Number: K171039
·
Decision Aug 29, 2017
Classifications
1
FEI Numbers
108
Registration Numbers
108
Same Product Code
84
Applicant Total
2
Review Days
145
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Basic Information
- Device Name
- Assut Filbloc Permanent Sutures
- K Number
- K171039
- Device Class
- FDA class 2
- Clearance Type
- Abbreviated
- Regulation Number
- 878.5010
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Assut Europe S.P.A.
- Date Received
- April 6, 2017
- Decision Date
- August 29, 2017
- Product Code
- GAW
- 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 |
|---|---|---|---|
| GAW | Suture, Nonabsorbable, Synthetic, Polypropylene | FDA class 2 | General, Plastic Surgery |
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Other Clearances by Assut Europe S.P.A.
| K Number | Device Name | ||
|---|---|---|---|
| K021767 | ASSUFIL | Nov 19, 2002 | Substantially Equivalent |