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

PTI ANNULOPLASTY RING(STERILE)

K Number: K905175 · Decision Feb 14, 1992
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
74
Applicant Total
19
Review Days
452

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Basic Information

Device Name
PTI ANNULOPLASTY RING(STERILE)
K Number
K905175
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.3800
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Pioneering Technologies, Inc.
Date Received
November 19, 1990
Decision Date
February 14, 1992
Product Code
KRH
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
KRH Ring, Annuloplasty

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K901815 MODIFIED STERILIZATION OF INTRA-ART(TM) CORONARY
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K901531 PTI INTRA-ARTR REUSABLE CORONARY ARTERY PROBE
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K897075 PTI INTRA-ART(TM) ANSARI SAPHENOUS VEIN HOLDER
K894684 PTI INTRA-ART INTERNAL MAMMARY ARTERY CANNULA KIT
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