FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MULTITAK SS SUTURE SYSTEM
K Number: K973015
·
Decision Oct 9, 1997
Classifications
1
FEI Numbers
275
Registration Numbers
275
Same Product Code
593
Applicant Total
5
Review Days
57
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Basic Information
- Device Name
- MULTITAK SS SUTURE SYSTEM
- K Number
- K973015
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3040
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Bonutti Research
- Date Received
- August 13, 1997
- Decision Date
- October 9, 1997
- Product Code
- MBI
- Advisory Committee
- Orthopedic
- Review Advisory Committee
- OR
- 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 |
|---|---|---|---|
| MBI | Fastener, Fixation, Nondegradable, Soft Tissue | FDA class 2 | Orthopedic |
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Other Clearances by Bonutti Research
| K Number | Device Name | ||
|---|---|---|---|
| K990156 | MULTITAK SS BUTTONS | Mar 5, 1999 | Substantially Equivalent |
| K971144 | MULTITAK SS SUTURE SYSTEM | Jun 25, 1997 | Substantially Equivalent |
| K964532 | MULTITAK SS SUTURE SYSTEM | Feb 3, 1997 | Substantially Equivalent |
| K964324 | MULTITAK SS SUTURE SYSTEM | Jan 10, 1997 | Substantially Equivalent |