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 | Device Class | Medical Specialty |
|---|---|---|---|
| OWY | Mesh, Surgical, Collagen, Orthopaedics, Reinforcement Of Tendon | FDA class 2 | General, Plastic Surgery |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (OWY), ordered by most recent decision date.
Arthrex SpeedFLEX Implant
FDA 510(k)
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Tapestry Biointegrative Implant
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TYBR Collagen Gel
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REGENETEN Bioinductive Implant
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Regeneten Bioinductive Implant
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Other Clearances by Embody, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K252647 | Tapestry Biointegrative Implant | Sep 19, 2025 | Substantially Equivalent |
| K223822 | ACTIVBRAID | Jun 2, 2023 | Substantially Equivalent |
| K220867 | Tapestry Biointegrative Implant | May 23, 2022 | Substantially Equivalent |
| K213958 | Bioabsorbable Anchor | Apr 8, 2022 | Substantially Equivalent |
| K201572 | TAPESTRY Biointegrative Implant | Oct 19, 2020 | Substantially Equivalent |