FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

HAV-LOK BUNION CORRECTION SYSTEM

K Number: K082384 · Decision Dec 8, 2008
Classifications
1
FEI Numbers
262
Registration Numbers
262
Same Product Code
88
Applicant Total
10
Review Days
111

Basic Information

Device Name
HAV-LOK BUNION CORRECTION SYSTEM
K Number
K082384
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
INSTRATEK, INC.
Date Received
August 19, 2008
Decision Date
December 8, 2008
Product Code
HTN
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HTN Washer, Bolt Nut

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