SONGER CABLE SYSTEM

Cerclage, Fixation

PIONEER SURGICAL TECHNOLOGY

The following data is part of a premarket notification filed by Pioneer Surgical Technology with the FDA for Songer Cable System.

Pre-market Notification Details

Device IDK922952
510k NumberK922952
Device Name:SONGER CABLE SYSTEM
ClassificationCerclage, Fixation
Applicant PIONEER SURGICAL TECHNOLOGY 375 RIVER PARK CIRCLE Marquette,  MI  49855 -0627
ContactMatthew N Songer
CorrespondentMatthew N Songer
PIONEER SURGICAL TECHNOLOGY 375 RIVER PARK CIRCLE Marquette,  MI  49855 -0627
Product CodeJDQ  
CFR Regulation Number888.3010 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1992-06-18
Decision Date1993-02-23

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
00846468040932 K922952 000
00846468040796 K922952 000
00846468040802 K922952 000
00846468040819 K922952 000
00846468040826 K922952 000
00846468040833 K922952 000
00846468040840 K922952 000
00846468040857 K922952 000
00846468040864 K922952 000
00846468040871 K922952 000
00846468040888 K922952 000
00846468016005 K922952 000

Trademark Results [SONGER CABLE SYSTEM]

Mark Image

Registration | Serial
Company
Trademark
Application Date
SONGER CABLE SYSTEM
SONGER CABLE SYSTEM
74164316 1838614 Dead/Cancelled
PIONEER LABORATORIES, INC.
1991-05-06

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