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

ISLAND BIOSURGICAL INC. BNS KIT #1 & #2

K Number: K973022 · Decision Oct 20, 1997
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
64
Applicant Total
3
Review Days
67

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Basic Information

Device Name
ISLAND BIOSURGICAL INC. BNS KIT #1 & #2
K Number
K973022
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.3300
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Island Biosurgical, Inc.
Date Received
August 14, 1997
Decision Date
October 20, 1997
Product Code
OTN
Advisory Committee
General, Plastic Surgery
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
OTN Mesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Retropubic Or Transobturator

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (OTN), ordered by most recent decision date.

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Other Clearances by Island Biosurgical, Inc.

K Number Device Name
K982042 ISLAND BIOSURGICAL BLADDER NECK BOLSTR MODEL IBIBOL.002
K960101 ISLAND BIOSURGICAL BOLSTER