FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MODIFICATION TO STRYKER XCEL ANCHOR SYSTEM
K Number: K041307
·
Decision Jun 14, 2004
Classifications
1
FEI Numbers
147
Registration Numbers
147
Same Product Code
219
Applicant Total
101
Review Days
28
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Basic Information
- Device Name
- MODIFICATION TO STRYKER XCEL ANCHOR SYSTEM
- K Number
- K041307
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 888.3030
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Stryker Endoscopy
- Date Received
- May 17, 2004
- Decision Date
- June 14, 2004
- Product Code
- MAI
- 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 |
|---|---|---|---|
| MAI | Fastener, Fixation, Biodegradable, Soft Tissue | FDA class 2 | Orthopedic |
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