510(k) K831041

SAGITTAL KNEE TESTER by Orthopedic Systems, Inc. — Product Code FTY

K831041 is an FDA 510(k) premarket notification submitted by Orthopedic Systems, Inc. for the device "SAGITTAL KNEE TESTER". The FDA issued a decision of Substantially Equivalent on June 24, 1983. The device falls under product code FTY (Tape, Measuring, Rulers And Calipers), a Class I device regulated under 21 CFR 878.4800. Orthopedic Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 24, 1983
Date Received
March 31, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Tape, Measuring, Rulers And Calipers
Device Class
Class I
Regulation Number
878.4800
Review Panel
SU
Submission Type