FDA 510(k) FDA class 3 Substantially Equivalent 🇺🇸 United States

PCA(R) SOLID BACK ACETABULA SHELL

K Number: K930833 · Decision Feb 22, 1994
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
44
Applicant Total
373
Review Days
370

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
PCA(R) SOLID BACK ACETABULA SHELL
K Number
K930833
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
888.3320
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Howmedica Corp.
Date Received
February 17, 1993
Decision Date
February 22, 1994
Product Code
JDL
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JDL Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JDL), ordered by most recent decision date.

View all

Other Clearances by Howmedica Corp.

K Number Device Name
K983528 MICRO DYNAMIC MESH
K983404 TYPE 3 FEMORAL COMPONENTS
K980925 DURATION II TIBIAL INSERTS-ETHYLENE OXIDE STERILIZATION
K980926 DURATION II ACETABULAR COMPONENTS-ETHYLENE OXIDE STERILIZATION
K980632 DURATION II TIBIAL INSERTS - GAS PLASMA STERILIZATION
K980626 DURATION II ACETABULAR COMPONENTS-GAS PLASMA STERILIZATION
K983419 HOFFMANN II MIAMI POST
K982958 ZETA MULTIZONE LOCKING NAIL SYSTEM
K982873 ZETA MULTIZONE SCN LOCKING NAIL
K982531 HOWMEDICA LEIBINGER RESORBABLE FIXATION SYSTEM
Search all 373 clearances from Howmedica Corp. →