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Variants of OSTEOMARK by Ostex Intl., Inc.
2 variants
Key
Device
Device · Manufacturer · Authorizations
Verified
Verified
Status
Status
Regime
Regime
Registry
Registry
Class
Class
Osteomark
Ostex Intl., Inc.
·
,
United States
(FDA applicant)
FDA 510(k)
K961562
Active
Cleared 11 Jul 1996
Active
Regimes:
510(k)
Registry:
510(k)
Class
Class:
I
Osteomark
Ostex Intl., Inc.
·
,
United States
(FDA applicant)
FDA 510(k)
K980518
Active
Cleared 6 Mar 1998
Active
Regimes:
510(k)
Registry:
510(k)
Class
Class:
I
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