510(k) K941896

STEADMAN LIGAMENT GRAFT PASSER AND PROTECTOR by Depuy, Inc. — Product Code LXH

K941896 is an FDA 510(k) premarket notification submitted by Depuy, Inc. for the device "STEADMAN LIGAMENT GRAFT PASSER AND PROTECTOR". The FDA issued a decision of Substantially Equivalent on November 7, 1994. The device falls under product code LXH (Orthopedic Manual Surgical Instrument), a Class I device regulated under 21 CFR 888.4540. Depuy, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 7, 1994
Date Received
April 18, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Orthopedic Manual Surgical Instrument
Device Class
Class I
Regulation Number
888.4540
Review Panel
OR
Submission Type