Atlas FDA

BONE FIXATION NAIL

FDA 510(k) clearance K943855 · decided 1995-07-12

Clearance details

K-number
K943855
Device name
BONE FIXATION NAIL
Applicant
Acu Med, Inc.
Decision
Substantially Equivalent
Date received
1994-08-08
Decision date
1995-07-12
Days to decision
338 days
Clearance type
Traditional
Product code
JDS
Device class
2
Regulation number
888.3030
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Beaverton, OR, US
Third-party review
No
Expedited review
No

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CONVENTUS PHS SYSTEM (K141737)Conventus Orthopaedics, Inc.2015-04-08
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Recalls involving this device

No recalls on record reference this clearance.