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

STRYKER FEMORAL CANAL BRUSH, ACETABULAR BRUSH

K Number: K941605 · Decision Aug 5, 1994
Classifications
1
FEI Numbers
1106
Registration Numbers
1106
Same Product Code
57
Applicant Total
124
Review Days
126

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Basic Information

Device Name
STRYKER FEMORAL CANAL BRUSH, ACETABULAR BRUSH
K Number
K941605
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
888.4540
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Stryker Corp.
Date Received
April 1, 1994
Decision Date
August 5, 1994
Product Code
LXH
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
LXH Orthopedic Manual Surgical Instrument

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K133671 ICONIX ALL SUTURE ANCHORS
K122113 MEMORY METAL STAPLES, EASYCLIP
K122284 HOFFMANN 3
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