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

KIRSCHNER WIRE (K-WIRE) AND STEINMANN PIN

K Number: K961522 · Decision Sep 23, 1996
Classifications
1
FEI Numbers
283
Registration Numbers
283
Same Product Code
203
Applicant Total
10
Review Days
154

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Basic Information

Device Name
KIRSCHNER WIRE (K-WIRE) AND STEINMANN PIN
K Number
K961522
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Synvasive Technology, Inc.
Date Received
April 22, 1996
Decision Date
September 23, 1996
Product Code
HTY
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
HTY Pin, Fixation, Smooth

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K972508 SURGICAL BURS AND SURGICAL DRILL BITS
K950009 POWERGRIP(TM) COMPRESSION FIXATION DEVICE
K934336 SPINALPLANE
K933933 CEBOPLANE
K930573 SYNVASIVE CERAMIC SUTTING BLOCK
K932869 ARTHROPLANE
K931737 HEDLEYL INTRAMEDULLARY PREPARATION BRUSH