FDA 510(k)
Substantially Equivalent
🇺🇸 United States
PRE-STERILIZATION OF VITALLIUM ALLOY
K Number: K820218
·
Decision Jun 3, 1982
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
373
Review Days
128
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Basic Information
- Device Name
- PRE-STERILIZATION OF VITALLIUM ALLOY
- K Number
- K820218
- Clearance Type
- Traditional
- Decision
- Substantially Equivalent
- Applicant
- Howmedica Corp.
- Date Received
- January 26, 1982
- Decision Date
- June 3, 1982
- Advisory Committee
- Unknown
- Review Advisory Committee
- OR
- Third Party
- N
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