FDA 510(k)
Substantially Equivalent
🇺🇸 United States
MAYO ELBOW II
K Number: K843778
·
Decision Mar 5, 1985
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
376
Review Days
161
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Basic Information
- Device Name
- MAYO ELBOW II
- K Number
- K843778
- Clearance Type
- Traditional
- Decision
- Substantially Equivalent
- Applicant
- Zimmer, Inc.
- Date Received
- September 25, 1984
- Decision Date
- March 5, 1985
- Advisory Committee
- Unknown
- Review Advisory Committee
- OR
- Third Party
- N
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