510(k) K241126

Device
OviTex PRS
Applicant
TELA Bio, Inc.
510(k) number
K241126
Product code
FTM
Decision
Substantially Equivalent (SESE)
Decision date
2024-05-22
Date received
2024-04-23
Regulation
878.3300
Classification name
Mesh, Surgical
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
John Urtz
Address
1 Great Valley Pkwy. Suite 24 Malvern PA US 19355 19355

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

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