FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
EUCLID REDUCTION AND GUIDANCE SYSTEM
K Number: K991037
·
Decision Jun 23, 1999
Classifications
1
FEI Numbers
115
Registration Numbers
115
Same Product Code
52
Applicant Total
2
Review Days
86
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Basic Information
- Device Name
- EUCLID REDUCTION AND GUIDANCE SYSTEM
- K Number
- K991037
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3030
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Modular Cutting Systems, Inc.
- Date Received
- March 29, 1999
- Decision Date
- June 23, 1999
- Product Code
- JDS
- 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 |
|---|---|---|---|
| JDS | Nail, Fixation, Bone | FDA class 2 | Orthopedic |
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Other Clearances by Modular Cutting Systems, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K990816 | AVCORE SYSTEM | Sep 24, 1999 | Substantially Equivalent |