FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MICROSTRIKE AND ALLTHREAD PEEK SUTURE ANCHOR
K Number: K060693
·
Decision Jun 6, 2006
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
17
Review Days
83
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Basic Information
- Device Name
- MICROSTRIKE AND ALLTHREAD PEEK SUTURE ANCHOR
- K Number
- K060693
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3040
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Arthrotek, Inc.
- Date Received
- March 15, 2006
- Decision Date
- June 6, 2006
- Product Code
- HWC
- 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 |
|---|---|---|---|
| HWC | Screw, Fixation, Bone | FDA class 2 | Orthopedic |
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|---|---|---|---|
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| K042460 | TI - SCREW ANCHOR SP | Oct 29, 2004 | Substantially Equivalent |
| K041274 | RESORBABLE INTERFERENCE SCREW | Jul 28, 2004 | Substantially Equivalent |
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| K040604 | INNERVUE DIAGNOSTIC SCOPE SYSTEM | Jun 4, 2004 | Substantially Equivalent |