Atlas FDA

ADSON-BECKMAN RETRACTOR, SPINAL

FDA 510(k) clearance K905445 · decided 1991-01-25

Clearance details

K-number
K905445
Device name
ADSON-BECKMAN RETRACTOR, SPINAL
Applicant
A. Henniss
Decision
Substantially Equivalent
Date received
1990-12-04
Decision date
1991-01-25
Days to decision
52 days
Clearance type
Traditional
Product code
GZT
Device class
2
Regulation number
882.4800
Medical specialty
Neurology
Advisory committee
Neurology
Location
Tarzana, CA, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.