FDA 510(k)
FDA unclassified
Substantially Equivalent
🇺🇸 United States
AESCULAP BONE WAX
K Number: K000021
·
Decision Mar 24, 2000
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
41
Applicant Total
207
Review Days
80
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Basic Information
- Device Name
- AESCULAP BONE WAX
- K Number
- K000021
- Device Class
- FDA unclassified
- Clearance Type
- Traditional
- Medical Specialty
- Unknown
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Aesculap, Inc.
- Date Received
- January 4, 2000
- Decision Date
- March 24, 2000
- Product Code
- MTJ
- Advisory Committee
- Unknown
- Review Advisory Committee
- SU
- 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 |
|---|---|---|---|
| MTJ | Wax, Bone | FDA unclassified | Unknown |
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·Unknown
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