510(k) K882671

SAMUELSON SCREWLOC CUP by Protek, Inc. — Product Code KWA

K882671 is an FDA 510(k) premarket notification submitted by Protek, Inc. for the device "SAMUELSON SCREWLOC CUP". The FDA issued a decision of Substantially Equivalent on October 20, 1988. The device falls under product code KWA (Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)), a Class III device regulated under 21 CFR 888.3330. Protek, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 20, 1988
Date Received
June 28, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)
Device Class
Class III
Regulation Number
888.3330
Review Panel
OR
Submission Type