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

Tapestry Biointegrative Implant

K Number: K212306 · Decision Nov 2, 2021
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
13
Applicant Total
6
Review Days
102

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Basic Information

Device Name
Tapestry Biointegrative Implant
K Number
K212306
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
Embody, Inc.
Date Received
July 23, 2021
Decision Date
November 2, 2021
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

Similar 510(k) Clearances

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

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Other Clearances by Embody, Inc.

K Number Device Name
K252647 Tapestry Biointegrative Implant
K223822 ACTIVBRAID™
K220867 Tapestry Biointegrative Implant
K213958 Bioabsorbable Anchor
K201572 TAPESTRY Biointegrative Implant