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

IFS BONE FIXATION DEVICES

K Number: K071035 · Decision Aug 13, 2007
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
4
Review Days
123

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Basic Information

Device Name
IFS BONE FIXATION DEVICES
K Number
K071035
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Internal Fixation Systems, Inc.
Date Received
April 12, 2007
Decision Date
August 13, 2007
Product Code
HWC
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
HWC Screw, Fixation, Bone

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HWC), ordered by most recent decision date.

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Other Clearances by Internal Fixation Systems, Inc.

K Number Device Name
K113399 IFS SUBTALAR IMPLANT
K110086 IFS PROFILE PLATES, SCREWS, AND WASHERS
K061620 IFS CANNULATED BONE SCREW