Atlas FDA

PUIG MASSANA-SHILEY ANNULOPLASTY RING

FDA 510(k) clearance K801879 · decided 1980-12-16

Clearance details

K-number
K801879
Device name
PUIG MASSANA-SHILEY ANNULOPLASTY RING
Applicant
Shiley, Inc.
Decision
Substantially Equivalent
Date received
1980-08-06
Decision date
1980-12-16
Days to decision
132 days
Clearance type
Traditional
Product code
KRH
Device class
2
Regulation number
870.3800
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
BJORK-SHILEY CARDIAC VALVE (P780008/S013)Shiley, Inc.1986-10-31
BJORK-SHILEY CARDIAC VALVE (P780008/S014)Shiley, Inc.1985-04-09
BJORK-SHILEY CARDIAC VALVE (P780008/S015)Shiley, Inc.1984-11-26
BJORK-SHILEY CARDIAC VALVE (P780008/S011)Shiley, Inc.1984-05-15
BJORK-SHILEY CARDIAC VALVE (P780008/S007)Shiley, Inc.1983-05-20
BJORK-SHILEY CARDIAC VALVE (P780008/S005)Shiley, Inc.1982-02-05