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

STRATAFIX™ Spiral PRONOVA™ Unidirectional Knotless Tissue Control Device STRATAFIX™ Spiral PRONOVA™ Bidirectional Knotless Tissue Control Device

K Number: K253572 · Decision Mar 27, 2026
Classifications
1
FEI Numbers
108
Registration Numbers
108
Same Product Code
84
Applicant Total
204
Review Days
130

Basic Information

Device Name
STRATAFIX™ Spiral PRONOVA™ Unidirectional Knotless Tissue Control Device STRATAFIX™ Spiral PRONOVA™ Bidirectional Knotless Tissue Control Device
K Number
K253572
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.5010
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ETHICON, Inc.
Date Received
November 17, 2025
Decision Date
March 27, 2026
Product Code
GAW
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GAW Suture, Nonabsorbable, Synthetic, Polypropylene

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