510(k) K931676

S-ROM(R) ZTT(TM) ACETABULAR CUP-APICAL HOLE PLUG by Joint Medical Products Corp. — Product Code JDL

K931676 is an FDA 510(k) premarket notification submitted by Joint Medical Products Corp. for the device "S-ROM(R) ZTT(TM) ACETABULAR CUP-APICAL HOLE PLUG". The FDA issued a decision of Substantially Equivalent on May 18, 1994. The device falls under product code JDL (Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)), a Class III device regulated under 21 CFR 888.3320. Joint Medical Products Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 18, 1994
Date Received
April 6, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)
Device Class
Class III
Regulation Number
888.3320
Review Panel
OR
Submission Type