Atlas FDA

ORTHOPEDIC PACKS

FDA 510(k) clearance K951231 · decided 1995-12-01

Clearance details

K-number
K951231
Device name
ORTHOPEDIC PACKS
Applicant
Sterile Concepts, Inc.
Decision
Substantially Equivalent
Date received
1995-03-20
Decision date
1995-12-01
Days to decision
256 days
Clearance type
Traditional
Product code
GAN
Device class
2
Regulation number
878.4830
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Richmond, VA, 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
SSC'S PCL MONOFILAMENT SAS, VIOLET, COATED, MODEL TBD (K003015)Surgical Specialties Corp2000-12-15
MONOCRYL (POLIGLECAPRONE 25) SUTURE, UNDYED (K964072)ETHICON, Inc.1996-12-18
MONOCRYL (POLIGLECAPRONE 25) SUTURE, DYED (MODIFIED) (K960653)ETHICON, Inc.1996-03-28
ULA (POLIGLECAPRONE 251) SYNTHETIC ABSOR SUT, DYED (K920978)ETHICON, Inc.1994-02-15
DEXON II ABSORBABLE SURGICAL SUTURE, U.S.P. (K900198)American Cyanamid Co.1990-07-05
POLYSORB SYNTHETIC ABSORBABLE SUTURE (K895579)United States Surgical, A Division of Tyco Healthc1990-07-05

Recalls involving this device

No recalls on record reference this clearance.