FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CUTIVA Topical Skin Adhesive (RM1700); CUTIVA PLUS Skin Closure System (RM1739)
K Number: K250950
·
Decision Aug 4, 2025
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
35
Applicant Total
2
Review Days
129
Basic Information
- Device Name
- CUTIVA Topical Skin Adhesive (RM1700); CUTIVA PLUS Skin Closure System (RM1739)
- K Number
- K250950
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.4010
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Okapi Medical, LLC Dba Resivant Medical
- Date Received
- March 28, 2025
- Decision Date
- August 4, 2025
- Product Code
- MPN
- 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 |
|---|---|---|---|
| MPN | Tissue Adhesive For The Topical Approximation Of Skin | FDA class 2 | General, Plastic Surgery |
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Other Clearances by Okapi Medical, LLC Dba Resivant Medical
| K Number | Device Name | ||
|---|---|---|---|
| K234114 | CUTIVA(TM) Topical Skin Adhesive (RM-1700); CUTIVA(TM) PLUS Skin Closure System (RM-1739) | Aug 20, 2024 | Substantially Equivalent |