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FDA 510(k) Application Details - K221632
Device Classification Name
More FDA Info for this Device
510(K) Number
K221632
Device Name
Spine CAMPÖ
Applicant
Medical Metrics, Inc.
2121 Sage Road
Houston, TX 77056 US
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Contact
Kirk Johnson
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Regulation Number
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Classification Product Code
QIH
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More FDA Info for this Product Code
Date Received
06/06/2022
Decision Date
10/18/2022
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
RA - Radiology
Review Advisory Committee
RA - Radiology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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