510(k) K852699

FREEMAN ACETABULAR CUP by Advanced Biosearch Assn. — Product Code KWA

K852699 is an FDA 510(k) premarket notification submitted by Advanced Biosearch Assn. for the device "FREEMAN ACETABULAR CUP". The FDA issued a decision of Substantially Equivalent on September 5, 1985. 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. Advanced Biosearch Assn. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 5, 1985
Date Received
June 26, 1985
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