FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

COPAL® exchange G hip spacer; COPAL® G+V

K Number: K234028 · Decision Feb 15, 2024
Classifications
1
FEI Numbers
149
Registration Numbers
149
Same Product Code
106
Applicant Total
13
Review Days
57

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Basic Information

Device Name
COPAL® exchange G hip spacer; COPAL® G+V
K Number
K234028
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3360
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Heraeus Medical GmbH
Date Received
December 20, 2023
Decision Date
February 15, 2024
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 Heraeus Medical GmbH

K Number Device Name
K241674 OSTEOPAL® V
K222570 COPAL knee moulds
K220492 COPAL exchange G hip spacer
K213812 PALACOS MV pro
K210607 PALACOS R pro, PALACOS R+G pro, PALACOS MV+G pro
K202475 PALACOS R, PALACOS R pro, PALACOS R+G, PALACOS R+G pro, PALACOS MV+G
K191016 COPAL exchange G Hip and Knee Spacers
K190766 PALACOS fast R+G
K182260 PALACOS MV
K153737 OSTEOPAL plus
Search all 13 clearances from Heraeus Medical GmbH →