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

INNOVASIVE DEVICES Y-KNOT SUTURE CLIP

K Number: K973313 · Decision Dec 1, 1997
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
69
Applicant Total
34
Review Days
89

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Basic Information

Device Name
INNOVASIVE DEVICES Y-KNOT SUTURE CLIP
K Number
K973313
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Innovasive Devices, Inc.
Date Received
September 3, 1997
Decision Date
December 1, 1997
Product Code
OCW
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
OCW Endoscopic Tissue Approximation Device

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Other Clearances by Innovasive Devices, Inc.

K Number Device Name
K994269 TITAN RC TACK
K993975 ABSOLUTE ABSORBABLE INTERFERENCE SCREW
K992458 RC MULTISUTURE BONE ANCHOR, MODEL 4453/4454
K992377 RC TACK
K990454 BIO-INTERFERENCE SCREW
K984490 SUTURELESS ANCHOR
K983560 INNOVASIVE DEVICES INTRATUNNEL TIBIAL FIXATION FASTENER
K983056 INNOVASIVE TIBIAL FASTENER
K981340 INNOVASIVE DEVICES MENISCAL DART REPAIR SYSTEM
K981193 INNOVASIVE 3.5MM METAL ROC XS SUTURE BONE FASTENER
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