Atlas FDA

ROBINSON MIDDLE EAR PROSTHESIS

FDA 510(k) clearance K760570 · decided 1976-09-21

Clearance details

K-number
K760570
Device name
ROBINSON MIDDLE EAR PROSTHESIS
Applicant
Xomed, Inc.
Decision
Substantially Equivalent
Date received
1976-09-01
Decision date
1976-09-21
Days to decision
20 days
Clearance type
Traditional
Product code
EIB
Device class
1
Regulation number
872.4565
Medical specialty
Dental
Advisory committee
Dental
Location
Arnold, MO, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
DTF-1000LL,DTF-1000 (K911118)Cp Medical1991-11-20
MODEL OPO-32 IRRIGATION SLEEVE (K874543)Allergan, Inc.1988-01-14
SYSTEM 80 FACEPLATE-IN-THE-EAR #F1 (K822411)Western Advanced Technology, Inc.1983-07-12

Recalls involving this device

No recalls on record reference this clearance.