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Baumer Muller Hip Prosthesis

by Baumer, S.A Brazil 510(k)

510(k) K003976

Product code JDI

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK003976 Date19 Mar 2001ClearedStatusActive

Coverage

1 jurisdiction

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  • Active
  • Not covered

United States — FDA 510(k) Active

Recalls: none on record (FDA, checked 22 Oct 2026)

Specification

510(k) · synced 22 Oct 2026

510(k) Number
FDA Product Code
JDI
Device Class
Class II
Regulation
21 CFR Part 888.3350
Advisory Committee
Orthopedic
FDA Decision
SESE Substantially Equivalent

Other devices from Baumer, S.A

Properties & raw data

Show properties, registry sources and raw records

Sources (1)

  • FDA 510(k) K003976 24 fields · synced 22 Oct 2026