510(k) K001922

DEPUY NEUFLEX PIP FINGER by Depuy, Inc. — Product Code KYJ

K001922 is an FDA 510(k) premarket notification submitted by Depuy, Inc. for the device "DEPUY NEUFLEX PIP FINGER". The FDA issued a decision of Substantially Equivalent on August 29, 2000. The device falls under product code KYJ (Prosthesis, Finger, Constrained, Polymer), a Class II device regulated under 21 CFR 888.3230. Depuy, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 29, 2000
Date Received
June 23, 2000
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Prosthesis, Finger, Constrained, Polymer
Device Class
Class II
Regulation Number
888.3230
Review Panel
OR
Submission Type