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

FEMORAL HEADS/MODULAR & FIXED W/ TITAN NITRIDE SUR

K Number: K892059 · Decision Jul 19, 1989
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
7
Applicant Total
25
Review Days
112

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Basic Information

Device Name
FEMORAL HEADS/MODULAR & FIXED W/ TITAN NITRIDE SUR
K Number
K892059
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3360
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Protek, Inc.
Date Received
March 29, 1989
Decision Date
July 19, 1989
Product Code
LZY
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
LZY Prosthesis, Hip, Hemi-, Femoral, Metal Ball

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LZY), 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
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. →