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

SBI STAFIX

K Number: K071479 · Decision Aug 2, 2007
Classifications
1
FEI Numbers
245
Registration Numbers
245
Same Product Code
230
Applicant Total
20
Review Days
65

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Basic Information

Device Name
SBI STAFIX
K Number
K071479
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Small Bone Innovations, Inc.
Date Received
May 29, 2007
Decision Date
August 2, 2007
Product Code
JDR
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
JDR Staple, Fixation, Bone

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Other Clearances by Small Bone Innovations, Inc.

K Number Device Name
K130147 ANATOMIC ANKLE ARTHRODESIS INTERLOCKING NAIL (A3 INTERLOCKING NAIL)
K112982 ANATOMIC ANKLE ARTHRODESIS INTERLOCKING NAIL(A3 INTERLOCKING NAIL )
K102180 RHEAD RADIAL HEAD EXTENDED STEMS
K092754 SBI FOOT AND ANKLE CANNULATED SCREW SYSTEM, MODEL 100-0061
K093550 MINI RAIL EXTERNAL FIXATOR SYSTEM
K073635 SBI SR MTP TOE IMPLANT
K071541 SBI TWISTOFIX
K063635 SBI FOREFOOT SET
K071656 SBI ARTFIX
K071540 SBI TITANIUM THREADED PIN
Search all 20 clearances from Small Bone Innovations, Inc. →