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

PARK CITY SHOULDER POSITIONER

K Number: K910031 · Decision Jan 24, 1991
Classifications
1
FEI Numbers
162
Registration Numbers
162
Same Product Code
60
Applicant Total
95
Review Days
20

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Basic Information

Device Name
PARK CITY SHOULDER POSITIONER
K Number
K910031
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 4, 1991
Decision Date
January 24, 1991
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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Other Clearances by Orthopedic Systems, Inc.

K Number Device Name
K952495 ANCHORS AWAY SOFT TISSUE ATTACHMENT SYSTEM
K920256 SPINE MOTION ANALYZER WITH EMG
K910736 JACKSON MULTIPURPOSE OPERATING TABLE
K903938 C FIT CUP
K892503 NUFFIELD TOTAL KNEE
K896678 SILICONE PLUG
K894283 COMPREHENSIVE SPINE MOTION ANALYZER
K890498 FREEMAN MODULAR HIP STEM RIDGED VERSION
K890331 FREEMAN TOTAL HIP SYSTEM RIDGED STEM
K895217 CORTICAL SCREW
Search all 95 clearances from Orthopedic Systems, Inc. →