Philippines FDA registration MDR-10178A

ARTHREX FASTHREAD PEEK INTERFERENCE SCREW, WITH DISPOSABLE SHEATH

Name: ARTHREX FASTHREAD PEEK INTERFERENCE SCREW, WITH DISPOSABLE SHEATH — Philippines FDA registration MDR-10178A
Creator: Arthrex, Inc.
Keywords: ARTHREX FASTHREAD PEEK INTERFERENCE SCREW, WITH DISPOSABLE SHEATH, MDR-10178A, Arthrex, Inc., Pacific Surgical, Inc., USA, Philippines FDA registration

PhilippinesArthrex, Inc.USAIssued August 06, 2020 – August 06, 2021

VerifiedFDA Philippines · official registry

Device information

Product Name: ARTHREX FASTHREAD PEEK INTERFERENCE SCREW, WITH DISPOSABLE SHEATH
Registration Number: MDR-10178A

Manufacturer details

Manufacturer: Arthrex, Inc.
Country of Origin: USA

Importer & distribution

Importer/Distributor: Pacific Surgical, Inc.

Registration dates

Issuance Date: August 06, 2020
Expiry Date: August 06, 2021

About this record

Access comprehensive regulatory information for ARTHREX FASTHREAD PEEK INTERFERENCE SCREW, WITH DISPOSABLE SHEATH in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10178A and manufactured by Arthrex, Inc. in USA. The device was registered on August 06, 2020.

This page provides complete registration details including manufacturer information, importer/distributor details (Pacific Surgical, Inc.), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.