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

Cryo 7

K Number: K220020 · Decision Feb 4, 2022
Classifications
1
FEI Numbers
478
Registration Numbers
480
Same Product Code
2867
Applicant Total
13
Review Days
30

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
Cryo 7
K Number
K220020
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Zimmer Medizinsysteme GmbH
Date Received
January 5, 2022
Decision Date
February 4, 2022
Product Code
GEX
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GEX Powered Laser Surgical Instrument

Similar 510(k) Clearances

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

View all

Other Clearances by Zimmer Medizinsysteme GmbH

K Number Device Name
K253408 CoolTone
K251378 CoolTone
K240347 PTG-05
K240178 RFG-01
K230780 MFG-05
K213256 ThermoTK
K222912 c1Trac
K220601 CoolTone
K203488 emField
K192940 CoolTone
Search all 13 clearances from Zimmer Medizinsysteme GmbH →