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

LITHOTOMY HOLDERS

K Number: K870098 · Decision Feb 6, 1987
Classifications
1
FEI Numbers
174
Registration Numbers
174
Same Product Code
60
Applicant Total
95
Review Days
28

Basic Information

Device Name
LITHOTOMY HOLDERS
K Number
K870098
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4950
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
ORTHOPEDIC SYSTEMS, INC.
Date Received
January 9, 1987
Decision Date
February 6, 1987
Product Code
FWZ
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
FWZ Operating Room Accessories Table Tray

Similar 510(k) Clearances

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K Number Device Name
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K910736 JACKSON MULTIPURPOSE OPERATING TABLE
K910031 PARK CITY SHOULDER POSITIONER
K903938 C FIT CUP
K892503 NUFFIELD TOTAL KNEE
K896678 SILICONE PLUG
K894283 COMPREHENSIVE SPINE MOTION ANALYZER
K890331 FREEMAN TOTAL HIP SYSTEM RIDGED STEM
K890498 FREEMAN MODULAR HIP STEM RIDGED VERSION
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