The following data is part of a premarket notification filed by Pioneer Surgical Technology with the FDA for Songer Cable System.
Device ID | K922952 |
510k Number | K922952 |
Device Name: | SONGER CABLE SYSTEM |
Classification | Cerclage, Fixation |
Applicant | PIONEER SURGICAL TECHNOLOGY 375 RIVER PARK CIRCLE Marquette, MI 49855 -0627 |
Contact | Matthew N Songer |
Correspondent | Matthew N Songer PIONEER SURGICAL TECHNOLOGY 375 RIVER PARK CIRCLE Marquette, MI 49855 -0627 |
Product Code | JDQ |
CFR Regulation Number | 888.3010 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-06-18 |
Decision Date | 1993-02-23 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
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 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SONGER CABLE SYSTEM 74164316 1838614 Dead/Cancelled |
PIONEER LABORATORIES, INC. 1991-05-06 |