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

Tapestry Biointegrative Implant

K Number: K252647 · Decision Sep 19, 2025
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
13
Applicant Total
6
Review Days
29

Basic Information

Device Name
Tapestry Biointegrative Implant
K Number
K252647
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.3300
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Embody, Inc.
Date Received
August 21, 2025
Decision Date
September 19, 2025
Product Code
OWY
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
OWY Mesh, Surgical, Collagen, Orthopaedics, Reinforcement Of Tendon

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K Number Device Name
K223822 ACTIVBRAID™
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K201572 TAPESTRY Biointegrative Implant