Sofamor Danek Mfg., Inc.
Sofamor Danek Mfg., Inc. holds FDA 510(k) medical device clearances, first cleared 1992, most recent 1995.
Top product codes for Sofamor Danek Mfg., Inc.
Recent clearances by Sofamor Danek Mfg., Inc.
- K936294 — SENTRY(TM) ANTERIOR/POSTERIOR SPINAL SYSTEMS
- K930191 — DANEK(TM) SPINAL EPIDURAL ENDOSCOPIC SY
- K932029 — TSRH SPINAL SCREWS
- K922486 — DANEK TISSUE CUTTING AND REMOVAL SYSTEM
- K930710 — SENTRY POSTERIOR SPINAL SYSTEM
- K930807 — SENTRY ANTERIOR SPINAL SYSTEM
- K922543 — Z-PLATE ANTERIOR FIXATION SYSTEM
- K923242 — CROSSLINK AXIAL AND OFFSET PLATES
- K921256 — LUQUE V SPINAL SYSTEM
- K922672 — AUGMENT POSTERIOR SPINAL FIXATION SYSTEM
- K925811 — TSRH CENTRAL POST HOOKS
- K925577 — DANEK TISSUE RESECTING SYSTEM
- K925812 — TITANIUM SONGER CABLE SYSTEM
- K920118 — RESORABPLUG
- K920546 — PARAGON POSTERIOR SPINAL SYSTEM
- K923446 — STERILE DYNA LOK ANTERIOR PLATING SYSTEM
- K924085 — RECONSTRUCTION PLATE SYSTEM
- K922520 — MODIFIED TSRH CENTRAL POST HOOKS
- K922087 — ANTERIOR CERVICAL PLATE SYSTEM
- K923339 — TSRH L CONNECTOR -- MODIFICATION
- K914306 — TSRH(TM) LATERAL OFFSET PLATE
- K914966 — TSRH CENTRAL POST HOOKS
- K920201 — TITANIUM ALLOY SONGER CABLE SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.