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

P.S.A. FEMORAL HIP PROSTHESIS

K Number: K893959 · Decision Jul 25, 1989
Classifications
1
FEI Numbers
216
Registration Numbers
216
Same Product Code
98
Applicant Total
25
Review Days
54

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Basic Information

Device Name
P.S.A. FEMORAL HIP PROSTHESIS
K Number
K893959
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3390
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Protek, Inc.
Date Received
June 1, 1989
Decision Date
July 25, 1989
Product Code
KWY
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
KWY Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented

Similar 510(k) Clearances

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

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Other Clearances by Protek, Inc.

K Number Device Name
K893785 ARC-2F ACETABULAR CUP
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.
K884789 NEW JERSEY FEMORAL HIP PROSTHESIS FOR CEMENT APPLI
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. →