Atlas FDA

SPINAL MARKER

FDA 510(k) clearance K944188 · decided 1995-04-13

Clearance details

K-number
K944188
Device name
SPINAL MARKER
Applicant
Leibinger L.P.
Decision
Substantially Equivalent
Date received
1994-08-26
Decision date
1995-04-13
Days to decision
230 days
Clearance type
Traditional
Product code
LXH
Device class
1
Regulation number
888.4540
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Dallas, TX, US
Third-party review
No
Expedited review
No

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MICROPERFORATION INSTRUMENT (K001507)Smith & Nephew, Inc.2000-06-14
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STEADMAN LIGAMENT GRAFT PASSER AND PROTECTOR (K941896)Depuy, Inc.1994-11-07
HYPERFLEX FLEXIBLE GUIDEWIRES (K941711)Linvatec Corp.1994-08-26
STRYKER FEMORAL CANAL BRUSH, ACETABULAR BRUSH (K941605)Stryker Corp.1994-08-05
PUNCH SURGICAL (K933772)Mahe-Medizintechnik1994-02-01
SOFAMOR ORTHOPAEDIC INSTRUMENTS (K933242)Danek Medical, Inc.1994-01-28
BARRIER BONE WAX APPLICATOR (K934260)Phillips Pharmaceuticals, Inc.1994-01-26

Recalls involving this device

No recalls on record reference this clearance.