FDA 510(k) FDA class 2 Substantially Equivalent for Some Indications 🇺🇸 United States

NEW JERSEY FEMORAL HIP PROSTHESIS FOR CEMENT APPLI

K Number: K884789 · Decision Feb 8, 1989
Classifications
1
FEI Numbers
149
Registration Numbers
149
Same Product Code
106
Applicant Total
25
Review Days
85

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Basic Information

Device Name
NEW JERSEY FEMORAL HIP PROSTHESIS FOR CEMENT APPLI
K Number
K884789
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3360
Medical Specialty
Orthopedic
Decision
Substantially Equivalent for Some Indications
Applicant
Protek, Inc.
Date Received
November 15, 1988
Decision Date
February 8, 1989
Product Code
KWL
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
KWL Prosthesis, Hip, Hemi-, Femoral, Metal

Similar 510(k) Clearances

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

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Other Clearances by Protek, Inc.

K Number Device Name
K893785 ARC-2F ACETABULAR CUP
K893959 P.S.A. FEMORAL HIP PROSTHESIS
K892059 FEMORAL HEADS/MODULAR & FIXED W/ TITAN NITRIDE SUR
K883794 RESUBMITTED CLW ACETABULAR CUP W/SULMESH
K884952 VARIOUS FEMORAL HIP PROSTHESES W/SELF LOCK CERAMIC
K884889 MODIFIED O.E.C. UNIV. SELF-ALIGNING ACETA. COMP.
K890054 M.E.M. ACETABULAR CUP W/SULMESH FOR CEMENT APPLI.
K884888 MODIFIED NEW JERSEY ACETABULAR COMP. & BONE SCREWS
K882671 SAMUELSON SCREWLOC CUP
K874093 SLS-88 TOTAL HIP SYSTEM, ACETABULAR CUP
Search all 25 clearances from Protek, Inc. →