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

STRYKER FEMORAL CANAL SPONGE & ACETABULUM SPONGE

K Number: K955599 · Decision Feb 22, 1996
Classifications
1
FEI Numbers
211
Registration Numbers
211
Same Product Code
110
Applicant Total
124
Review Days
76

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Basic Information

Device Name
STRYKER FEMORAL CANAL SPONGE & ACETABULUM SPONGE
K Number
K955599
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4450
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Stryker Corp.
Date Received
December 8, 1995
Decision Date
February 22, 1996
Product Code
GDY
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GDY Gauze/Sponge, Internal, X-Ray Detectable

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