FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

SMILJANIC BONE REPOSITIONING FORCEPS

K Number: K871535 · Decision May 14, 1987
Classifications
1
FEI Numbers
658
Registration Numbers
658
Same Product Code
72
Applicant Total
21
Review Days
24

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Basic Information

Device Name
SMILJANIC BONE REPOSITIONING FORCEPS
K Number
K871535
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Link America, Inc.
Date Received
April 20, 1987
Decision Date
May 14, 1987
Product Code
HTD
Advisory Committee
General, Plastic Surgery
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
HTD Forceps

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