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Global Ap 1130-52-500

by Depuy Orthopaedics, Inc.

Global Ap 1130-52-500 (113052500) is a Class II device made by Depuy Orthopaedics, Inc., cleared under FDA 510(k) K060874 on 28 Jun 2006 and listed in FDA GUDID since 24 Sep 2015 (UDI-DI 10603295006220), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K060874

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10603295006220 UDI-DI Date24 Sep 2015ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK060874 Date28 Jun 2006DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K060874 decided 28 Jun 2006 Active
  • FDA GUDID UDI-DI 10603295006220 listed 24 Sep 2015 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K060874
  2. Listed FDA GUDID 10603295006220

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Global Ap
Generic name
Stem-fixed metallic humeral head prosthesis
Model / Ref / Catalog
1130-52-500, 113052500
Primary DI / UDI-DI
10603295006220
510(k) Number
FDA product code
HSD, KWS
GMDN term
Stem-fixed metallic humeral head prosthesis
Device class
Class II
Regulation number
888.3690, 888.3660
GUDID distribution status
In Commercial Distribution

Similar devices in this category

Other devices filed under Stem-fixed metallic humeral head prosthesis.

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Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)