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
MTJ Wax, Bone

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