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

DURA-GUARD - DURAL REPAIR PATCH

K Number: K982282 · Decision Jul 30, 1998
Classifications
1
FEI Numbers
40
Registration Numbers
40
Same Product Code
42
Applicant Total
26
Review Days
30

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Basic Information

Device Name
DURA-GUARD - DURAL REPAIR PATCH
K Number
K982282
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
882.5910
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bio-Vascular, Inc.
Date Received
June 30, 1998
Decision Date
July 30, 1998
Product Code
GXQ
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
GXQ Dura Substitute

Similar 510(k) Clearances

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

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Other Clearances by Bio-Vascular, Inc.

K Number Device Name
K002233 BVI SLING
K992537 PERI-STRIPS-SLEEVE, PERI-STRIPS-STRIP AND PERI-STRIPS DRY (NON-NAOH-TREATED AND NAOH-TREATED
K983602 CV PERI-GUARD AND VASCU-GUARD
K983581 OCU-GUARD AND OCU-GUARD SUPPLE
K983162 PERI-GUARD, CV PERI-GUARD, OCU-GUARD, SUPPLE PERI-GUARD, PERI-STRIPS - SLEEVE, PERI-STRIPS-STRIPS, PERI-STRIPS DRY, VASC
K981624 FLO-THRU
K971726 CV PERI-GUARD - CARDIOVASCULAR PATCH
K973706 DURA-GUARD-DURAL REPAIR PATCH
K973552 OCU-GUARD ORBITAL IMPLANT WRAP, SUPPLE OCU-GUARD ORBITAL IMPLANT WRAP
K971048 PERI-STRIPS DRY - STAPLE LINE REINFORCEMENT
Search all 26 clearances from Bio-Vascular, Inc. →