FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
VERSITOMIC ACL FLEXIBLE REAMER SYSTEM STERILIZATION TRAY
K Number: K100887
·
Decision Aug 9, 2010
Classifications
1
FEI Numbers
266
Registration Numbers
266
Same Product Code
279
Applicant Total
4
Review Days
132
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Basic Information
- Device Name
- VERSITOMIC ACL FLEXIBLE REAMER SYSTEM STERILIZATION TRAY
- K Number
- K100887
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.6850
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Tag Medical Products
- Date Received
- March 30, 2010
- Decision Date
- August 9, 2010
- Product Code
- KCT
- Advisory Committee
- General Hospital
- Review Advisory Committee
- HO
- 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 |
|---|---|---|---|
| KCT | Sterilization Wrap Containers, Trays, Cassettes & Other Accessories | FDA class 2 | General Hospital |
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