Flow-Screw™ 102-35-2022T

• FDA 510(k) K142776 decided 23 Mar 2015 Active
• FDA GUDID UDI-DI B267102013520220 listed 30 Jun 2017 Listed

1. 23 Mar 2015 Cleared FDA 510(k) K142776
2. 30 Jun 2017 Listed FDA GUDID B267102013520220

Trade name

Flow-Screw™

Generic name

Orthopaedic bone screw, non-bioabsorbable, non-sterile

Model / Ref / Catalog

102-35-2022T

Primary DI / UDI-DI

B267102013520220

510(k) Number

K142776 ↗

FDA product code

HWC

GMDN term

Orthopaedic bone screw, non-bioabsorbable, non-sterile

Device class

Class II

Regulation number

888.3040

GUDID distribution status

In Commercial Distribution

Sterilisation method

Moist Heat or Steam Sterilization

Category: Orthopaedic bone screw, non-bioabsorbable, non-sterile

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• Flow-FX 102-13-02

  Class I

  FDA 510(k) K142776 Active Cleared 23 Mar 2015 GUDID on market

• Flow-Screw™ 73-2035

  Class II

  FDA 510(k) K142776 Active Cleared 23 Mar 2015 GUDID on market

• Flow-Screw™ 102-65-1060T

  Class II

  FDA 510(k) K142776 Active Cleared 23 Mar 2015 GUDID on market

• Flow-Screw™ 55-2044

  Class II

  FDA 510(k) K142776 Active Cleared 23 Mar 2015 GUDID on market

See all devices from Flow-Fx, LLC →