Atlas FDA

CARDIOVASCULAR REPAIR PATCH

FDA 510(k) clearance K905073 · decided 1991-12-20

Clearance details

K-number
K905073
Device name
CARDIOVASCULAR REPAIR PATCH
Applicant
Impra, Inc.
Decision
Substantially Equivalent
Date received
1990-11-09
Decision date
1991-12-20
Days to decision
406 days
Clearance type
Traditional
Product code
DXZ
Device class
2
Regulation number
870.3470
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Tempe, AZ, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
PeriBeam® Pericardial Membrane (K240775)Tamabio2025-04-18
Vascutek Gelseal Patch, Vascutek Gelsoft Patch, Vascutek Thin Wall Carotid Patch (K200955)Vascutek, Ltd.2020-07-08
PhotoFix Decellularized Bovine Pericardium (K162506)Cryolife, Inc.2017-03-09
VascuCel (K162579)Admedus Regen Pty, Ltd.2016-10-14
CorMatrix Tyke (K152127)Cormatrix Cardiovascular, Inc.2016-02-04
PremiPatch PTFE Pledget (K151865)Aesculap, Inc.2015-10-27
PERI-GUARD Repair Patch & SUPPLE PERI-GUARD Repair Patch (K142447)Synovis Life Technologies, Inc.2015-01-07
VASCU-GUARD Peripheral Vascular Patch (K142461)Synovis Life Technologies, Inc.2014-11-25
CORMATRIX ECM FOR VASCULAR REPAIR (K140789)Cormatrix Cardiovascular, Inc.2014-07-15
CARDIOCEL (K130872)Celxcel Pty, Ltd.2014-01-30
SYNOVIS COLLAGEN MATRIX (TBD) (K122306)Synovis Surgical Innovations2013-03-08
SMI CARDIOVASCULAR PATCH (K122105)Solinas Medical, Inc.2012-12-07

Recalls involving this device

No recalls on record reference this clearance.